Human (GRCh38.p14)
Description

solute carrier family 2 member 4 [Source:HGNC Symbol;Acc:HGNC:11009]

Gene Synonyms

GLUT4

Location
About this transcript

This transcript has 11 exons, is annotated with 37 domains and features, is associated with 3439 variant alleles and maps to 558 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000317370.13SLC2A4-2013375509aaENSP00000320935.8
 
Protein coding
CCDS11097P14672-1 NM_001042.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000424875.2SLC2A4-2021852451aaENSP00000396887.2
 
Protein coding
F5H081 -GENCODE basicTSL:2
ENST00000571308.5SLC2A4-2041768461aaENSP00000459864.1
 
Protein coding
I3L2R4 -GENCODE basicTSL:5
ENST00000572485.5SLC2A4-2052995415aaENSP00000461086.1
 
Nonsense mediated decay
P14672-2 -TSL:1
ENST00000570783.5SLC2A4-2031813219aaENSP00000459056.1
 
Nonsense mediated decay
I3L1S2 -TSL:3
Statistics

Exons: 11, Coding exons: 11, Transcript length: 3,375 bps, Translation length: 509 residues

MANE

This MANE Select transcript contains ENSP00000320935 and matches to NM_001042.3 and NP_001033.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P14672

CCDS

This transcript is a member of the Human CCDS set: CCDS11097

Transcript Support Level (TSL)

TSL:1

Version

ENST00000317370.13

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.