Human (GRCh38.p14)
Description

solute carrier family 7 member 11 [Source:HGNC Symbol;Acc:HGNC:11059]

Gene Synonyms

XCT

About this transcript

This transcript has 12 exons, is annotated with 23 domains and features, is associated with 32062 variant alleles and maps to 654 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000280612.9SLC7A11-2019645501aaENSP00000280612.5
 
Protein coding
CCDS3742Q9UPY5 NM_014331.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000509248.1SLC7A11-20279775aaENSP00000424046.1
 
Nonsense mediated decay
H0Y9F9 -TSL:5CDS 5' incomplete
Statistics

Exons: 12, Coding exons: 12, Transcript length: 9,645 bps, Translation length: 501 residues

MANE

This MANE Select transcript contains ENSP00000280612 and matches to NM_014331.4 and NP_055146.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9UPY5

CCDS

This transcript is a member of the Human CCDS set: CCDS3742

Transcript Support Level (TSL)

TSL:1

Version

ENST00000280612.9

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.