Human (GRCh37.p13)
Description

solute carrier family 7 (neutral amino acid transporter light chain, asc system), member 10 [Source:HGNC Symbol;Acc:11058]

Gene Synonyms

ASC1, HASC-1, asc-1

Location

Chromosome 19: 33,699,570-33,716,756 reverse strand.

GRCh37:CM000681.1

About this gene

This gene has 5 transcripts (splice variants) and 7 paralogues.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000253188.4SLC7A10-0011946523aa
 
Protein coding
CCDS12431Q9NS82 NM_019849.2Ensembl CanonicalGENCODE Basic
ENST00000590036.1SLC7A10-0051641389aa
 
Nonsense mediated decay
K7EK24 --
ENST00000592596.1SLC7A10-002143171aa
 
Nonsense mediated decay
K7ENB6 --
ENST00000587064.1SLC7A10-00378971aa
 
Nonsense mediated decay
K7ENB6 --
ENST00000590490.1SLC7A10-0041462No protein
 
Retained intron
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Name

SLC7A10 (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: Q9NS82

CCDS

This gene is a member of the Human CCDS set: CCDS12431.1

Ensembl version

ENSG00000130876.7

Other assemblies

This gene maps to 33,208,664-33,225,850 in GRCh38 coordinates.

Gene type

Protein coding

Annotation method

Annotation for this gene includes both automatic annotation from Ensembl and Havana manual curation, see article.

Alternative genes

This gene corresponds to the following database identifiers:

Havana gene:
OTTHUMG00000180344 (version 3)

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