neurotrophin 3 [Source:VGNC Symbol;Acc:VGNC:32299]
Primary_assembly 5: 104,745,602-104,823,230 reverse strand.
This transcript has 2 exons, is annotated with 24 domains and features and is associated with 3906 variant alleles.
This transcript is a product of gene ENSBTAG00000010223.7 Show transcript tableHide transcript table
| Transcript ID | Name | bp | Protein | Translation ID | Biotype | UniProt Match | Flags |
|---|---|---|---|---|---|---|---|
| ENSBTAT00000013493.7 | NTF3-201 | 2395 | 266aa | ENSBTAP00000040469.4 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0AAF6ZED4 | 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, APPRIS ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1, |
| ENSBTAT00000127907.1 | NTF3-207 | 1872 | 253aa | ENSBTAP00000097188.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q08DT3 | APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2, |
| ENSBTAT00000107230.1 | NTF3-203 | 1605 | 253aa | ENSBTAP00000078815.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q08DT3 | APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2, |
| ENSBTAT00000124140.1 | NTF3-202 | 1392 | 253aa | ENSBTAP00000079651.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q08DT3 | APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2, |
| ENSBTAT00000133363.1 | NTF3-205 | 1318 | 253aa | ENSBTAP00000102991.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q08DT3 | APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2, |
| ENSBTAT00000111210.1 | NTF3-208 | 1255 | 253aa | ENSBTAP00000101763.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q08DT3 | APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2, |
| ENSBTAT00000098411.1 | NTF3-204 | 1247 | 253aa | ENSBTAP00000078842.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q08DT3 | APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2, |
| ENSBTAT00000126149.1 | NTF3-209 | 1087 | 248aa | ENSBTAP00000078847.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0AAA9S1H1 | - |
| ENSBTAT00000099539.1 | NTF3-206 | 1059 | 253aa | ENSBTAP00000084117.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q08DT3 | APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2, |