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Human (GRCh38.p14)
Description

solute carrier family 6 member 19 [Source:HGNC Symbol;Acc:HGNC:27960]

Gene Synonyms

B0AT1

Location

Chromosome 5: 1,201,595-1,225,111 forward strand.

GRCh38:CM000667.2

About this gene

This gene has 2 transcripts (splice variants), 353 orthologues, 19 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000304460.11SLC6A19-2015168634aaENSP00000305302.10
 
Protein coding
CCDS34130Q695T7 NM_001003841.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000515652.5SLC6A19-2023337354aaENSP00000425701.1
 
Nonsense mediated decay
E9PD72 -TSL:2