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 13 exons, is annotated with 20 domains and features, is associated with 19144 variant alleles and maps to 519 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: 13, Coding exons: 11, Transcript length: 1,819 bps, Translation length: 467 residues

MANE

This MANE Select transcript contains ENSP00000244527 and matches to NM_005074.5 and NP_005065.2

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:5

Version

ENST00000244527.10

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

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