Transcript: SLC32A1-201 ENST00000217420.1

Description

solute carrier family 32 member 1 [Source:HGNC Symbol;Acc:HGNC:11018]

Synonyms

VIAAT, VGAT, bA122O1.1

Location

About this transcript

This transcript has 2 exons, is annotated with 13 domains and features, is associated with 409 variations and maps to 199 oligo probes.

Gene

Name	Transcript ID	bp	Protein	Translation ID	Biotype	CCDS	UniProt	RefSeq	Flags
SLC32A1-201	ENST00000217420.1	2574	525aa	ENSP00000217420	<p>Genes and/or transcript that contains an open reading frame (ORF).</p>Protein coding	CCDS13307	Q9H598	NM_080552 NP_542119	<p>Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.</p><p>The <a href="https://genome.ucsc.edu/cgi-bin/hgc?hgsid=423831555_sqRhAapgi8atmzzBPBAz8Me5797J&c=chr14&o=94517268&t=94547548&g=wgEncodeGencodeCompV19&i=ENST00000544005.1#tsl" target="_self">Transcript Support Level</a> (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.</p>TSL:1The GENCODE set is the gene set for human and mouse. <a href="/Help/Glossary?id=500" class="popup">GENCODE Basic</a> is a subset of representative transcripts (splice variants).GENCODE basic<p>PRINCIPAL1 - APPRIS candidate principal isoform.</p><p><a class="popup" href="/Homo_sapiens/Help/Glossary?id=521">APPRIS</a> is a system to annotate alternatively spliced transcripts based on a range of computational methods.</p>APPRIS P1

Variants