Human (GRCh38.p14)
Description

solute carrier family 17 member 1 [Source:HGNC Symbol;Acc:HGNC:10929]

Gene Synonyms

NAPI-1, NPT1

Location
About this transcript

This transcript has 12 exons, is annotated with 20 domains and features, is associated with 13528 variant alleles and maps to 467 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000244527.10SLC17A1-2011819467aaENSP00000244527.4
 
Protein coding
CCDS4565Q14916-1 NM_005074.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000476801.5SLC17A1-2041704467aaENSP00000420614.1
 
Protein coding
CCDS4565Q14916-1 -GENCODE basicAPPRIS P1TSL:2
ENST00000468082.1SLC17A1-2031242413aaENSP00000420546.1
 
Protein coding
Q14916-2 -GENCODE basicTSL:1
ENST00000377886.6SLC17A1-2021433209aaENSP00000367118.2
 
Nonsense mediated decay
E9PGW3 -TSL:5
Statistics

Exons: 12, Coding exons: 11, Transcript length: 1,704 bps, Translation length: 467 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q14916

CCDS

This transcript is a member of the Human CCDS set: CCDS4565

Transcript Support Level (TSL)

TSL:2

Version

ENST00000476801.5

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.