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Human (GRCh38.p14)
Description

solute carrier family 5 member 1 [Source:HGNC Symbol;Acc:HGNC:11036]

Gene Synonyms

D22S675, NAGT, SGLT-1, SGLT1

Location
About this transcript

This transcript has 15 exons, is annotated with 63 domains and features, is associated with 28807 variant alleles and maps to 808 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000266088.9SLC5A1-2014832664aaENSP00000266088.4
 
Protein coding
CCDS13902P13866-1 NM_000343.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000543737.2SLC5A1-2044752537aaENSP00000444898.1
 
Protein coding
CCDS58805P13866-2 -GENCODE BasicTSL:2
ENST00000477969.1SLC5A1-202801No protein-
 
Retained intron
--TSL:3
ENST00000486394.1SLC5A1-203568No protein-
 
Retained intron
--TSL:4
Statistics

Exons: 15, Coding exons: 15, Transcript length: 4,832 bps, Translation length: 664 residues

MANE

This MANE Select transcript contains ENSP00000266088 and matches to NM_000343.4 and NP_000334.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P13866

CCDS

This transcript is a member of the Human CCDS set: CCDS13902

Transcript Support Level (TSL)

TSL:1

Version

ENST00000266088.9

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.

GENCODE primary gene

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