serine and arginine rich splicing factor 2a [Source:ZFIN;Acc:ZDB-GENE-040426-2706]
Chromosome 12: 31,722,612-31,724,343 reverse strand.
This transcript has 2 exons, is associated with 141 variant alleles and maps to 152 oligo probes.
This transcript is a product of gene ENSDARG00000057484.8 Show transcript tableHide transcript table
| Transcript ID | Name | bp | Protein | Translation ID | Biotype | UniProt Match | Flags |
|---|---|---|---|---|---|---|---|
| ENSDART00000080173.6 | srsf2a-201 | 1776 | 225aa | ENSDARP00000074623.4 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q7ZV13 | 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 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, |
| ENSDART00000137464.2 | srsf2a-204 | 1151 | 174aa | ENSDARP00000115120.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | - | APPRIS ALT2: 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 appear to be conserved in fewer than 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 ALT2, |
| ENSDART00000153056.3 | srsf2a-207 | 855 | 199aa | ENSDARP00000127296.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | - | 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete, |
| ENSDART00000165299.2 | srsf2a-211 | 788 | 225aa | ENSDARP00000135738.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q7ZV13 | 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, |
| ENSDART00000153174.2 | srsf2a-209 | 707 | 118aa | ENSDARP00000127448.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | - | 3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete, |
| ENSDART00000153102.3 | srsf2a-208 | 908 | 148aa | ENSDARP00000127145.1 | Nonsense mediated decay | - | 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete, |
| ENSDART00000146446.3 | srsf2a-206 | 603 | 13aa | ENSDARP00000127111.1 | Nonsense mediated decay | - | 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete, |
| ENSDART00000132753.2 | srsf2a-202 | 582 | 47aa | ENSDARP00000127367.1 | Nonsense mediated decay | - | 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete, |
| ENSDART00000140550.2 | srsf2a-205 | 567 | 85aa | ENSDARP00000127259.1 | Nonsense mediated decay | - | 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete, |
| ENSDART00000136278.3 | srsf2a-203 | 1024 | No protein | - | An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron | - | - |
| ENSDART00000153210.2 | srsf2a-210 | 636 | No protein | - | An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron | - | - |