Human (GRCh37.p13)
Description

solute carrier family 6 (neutral amino acid transporter), member 19 [Source:HGNC Symbol;Acc:27960]

Gene Synonyms

B0AT1, HND

Location

Chromosome 5: 1,201,710-1,225,232 forward strand.

GRCh37:CM000667.1

About this gene

This gene has 2 transcripts (splice variants), 5 paralogues and is associated with 6 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000304460.10SLC6A19-0015174634aaENSP00000305302.10
 
Protein coding
CCDS34130B3KVZ8 Q695T7 NM_001003841.2GENCODE basic
ENST00000515652.1SLC6A19-0023337354aaENSP00000425701.1
 
Nonsense mediated decay
E9PD72 --