Human (GRCh38.p14)
Description

solute carrier family 5 member 3 [Source:HGNC Symbol;Acc:HGNC:11038]

Gene Synonyms

SMIT, SMIT1

Location
About this transcript

This transcript has 2 exons, is annotated with 25 domains and features, is associated with 15341 variant alleles and maps to 560 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000381151.5SLC5A3-20111566718aaENSP00000370543.3
 
Protein coding
CCDS33549P53794 NM_006933.7MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
Statistics

Exons: 2, Coding exons: 1, Transcript length: 11,566 bps, Translation length: 718 residues

MANE

This MANE Select transcript contains ENSP00000370543 and matches to NM_006933.7 and NP_008864.4

Uniprot

This transcript corresponds to the following Uniprot identifiers: P53794

CCDS

This transcript is a member of the Human CCDS set: CCDS33549

Transcript Support Level (TSL)

TSL:1

Version

ENST00000381151.5

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.