Human (GRCh38.p14)
Description

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

Gene Synonyms

ASC-1

Location

Chromosome 19: 33,208,664-33,225,850 reverse strand.

GRCh38:CM000681.2

About this gene

This gene has 5 transcripts (splice variants), 298 orthologues and 12 paralogues.

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