Human (GRCh38.p14)
Description

solute carrier family 7 member 10 [Source:HGNC Symbol;Acc:HGNC:11058]

Gene Synonyms

ASC-1

Location
About this transcript

This transcript has 11 exons, is annotated with 21 domains and features, is associated with 9160 variant alleles and maps to 360 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000253188.8SLC7A10-2011946523aaENSP00000253188.2
 
Protein coding
CCDS12431Q9NS82 NM_019849.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000590036.5SLC7A10-2031641389aaENSP00000465421.1
 
Nonsense mediated decay
K7EK24 -TSL:5
ENST00000592596.1SLC7A10-205143171aaENSP00000466410.1
 
Nonsense mediated decay
K7ENB6 -TSL:1
ENST00000587064.5SLC7A10-20278971aaENSP00000466876.1
 
Nonsense mediated decay
K7ENB6 -TSL:3
ENST00000590490.1SLC7A10-2041462No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 11, Coding exons: 11, Transcript length: 1,946 bps, Translation length: 523 residues

MANE

This MANE Select transcript contains ENSP00000253188 and matches to NM_019849.3 and NP_062823.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9NS82

CCDS

This transcript is a member of the Human CCDS set: CCDS12431

Transcript Support Level (TSL)

TSL:1

Version

ENST00000253188.8

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.