Human (GRCh38.p14)
Description

solute carrier family 1 member 5 [Source:HGNC Symbol;Acc:HGNC:10943]

Gene Synonyms

AAAT, ASCT2, M7V1, RDRC

Location

Chromosome 19: 46,774,883-46,788,594 reverse strand.

GRCh38:CM000681.2

About this gene

This gene has 6 transcripts (splice variants), 193 orthologues and 6 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000542575.6SLC1A5-2032882541aaENSP00000444408.1
 
Protein coding
CCDS12692Q15758-1 NM_005628.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000594991.5SLC1A5-2052031365aaENSP00000469265.1
 
Protein coding
M0QXM4 -GENCODE basicTSL:2
ENST00000434726.6SLC1A5-2021872339aaENSP00000406532.1
 
Protein coding
CCDS46125Q15758-2 -GENCODE basicTSL:2
ENST00000412532.6SLC1A5-2011750313aaENSP00000397924.1
 
Protein coding
CCDS46126Q15758-3 -GENCODE basicTSL:2
ENST00000593713.1SLC1A5-204774258aaENSP00000468890.1
 
Protein coding
M0QX44 -TSL:3CDS 5' and 3' incomplete
ENST00000598022.1SLC1A5-20627629aaENSP00000471626.1
 
Protein coding
M0R144 -TSL:3CDS 3' incomplete