| ENSMUST00000232437.2 | Pacsin1-211 | 4566 | 441aa | ENSMUSP00000155999.2 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | CCDS28567 | Q543Y7 Q61644 | A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1, |
| ENSMUST00000231669.2 | Pacsin1-208 | 4209 | 441aa | ENSMUSP00000156003.2 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | CCDS28567 | Q543Y7 Q61644 | The GENCODE set is the gene set for human and mouse. is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1, |
| ENSMUST00000045896.11 | Pacsin1-201 | 4176 | 441aa | ENSMUSP00000044168.4 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | CCDS28567 | Q543Y7 Q61644 | The GENCODE set is the gene set for human and mouse. is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1, |
| ENSMUST00000114873.8 | Pacsin1-204 | 1857 | 441aa | ENSMUSP00000110523.2 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | CCDS28567 | Q543Y7 Q61644 | The GENCODE set is the gene set for human and mouse. is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1, |
| ENSMUST00000097360.3 | Pacsin1-202 | 1800 | 441aa | ENSMUSP00000094973.3 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | CCDS28567 | Q543Y7 Q61644 | The GENCODE set is the gene set for human and mouse. is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1, |
| ENSMUST00000114872.9 | Pacsin1-203 | 972 | 320aa | ENSMUSP00000110522.3 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | | A0A384DVB1 | TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete, |
| ENSMUST00000231236.2 | Pacsin1-206 | 672 | 109aa | ENSMUSP00000155877.2 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | | A0A338P6K4 | 3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete, |
| ENSMUST00000231350.2 | Pacsin1-207 | 1368 | No protein | - | Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined | | - | - |
| ENSMUST00000155259.2 | Pacsin1-205 | 552 | No protein | - | Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined | | - | TSL 2: A transcript where the best supporting mRNA is flagged as suspect or the support is from multiple ESTs The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:2, |
| ENSMUST00000231854.2 | Pacsin1-209 | 1786 | No protein | - | An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron | | - | - |
| ENSMUST00000232225.2 | Pacsin1-210 | 697 | No protein | - | An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron | | - | - |
