Human (GRCh38.p14)
Description

solute carrier family 2 member 13 [Source:HGNC Symbol;Acc:HGNC:15956]

Gene Synonyms

HMIT

Location
About this transcript

This transcript has 10 exons, is annotated with 35 domains and features, is associated with 148353 variant alleles and maps to 580 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000280871.9SLC2A13-2017221648aaENSP00000280871.4
 
Protein coding
CCDS8736Q96QE2 NM_052885.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000380858.1SLC2A13-2023082357aaENSP00000370239.1
 
Protein coding
E9PE47 -GENCODE basicTSL:1
ENST00000465517.1SLC2A13-2031026No protein-
 
Retained intron
--TSL:2
ENST00000505338.1SLC2A13-204436No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 10, Coding exons: 10, Transcript length: 7,221 bps, Translation length: 648 residues

MANE

This MANE Select transcript contains ENSP00000280871 and matches to NM_052885.4 and NP_443117.3

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96QE2

CCDS

This transcript is a member of the Human CCDS set: CCDS8736

Transcript Support Level (TSL)

TSL:1

Version

ENST00000280871.9

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.