Canonical Allele Identifier: CA1522519568

Gene: SLC6A19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1213018T= , CM000667.2:g.1213018T=	GRCh38
NC_000005.9:g.1213133T= , CM000667.1:g.1213133T=	GRCh37
NC_000005.8:g.1266133T=	NCBI36
NG_008282.1:g.16424T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304460.11:c.664-445T= MANE Select	ENSP00000305302.10:n.664-445T=
ENST00000304460.10:c.664-445T=	ENSP00000305302.10:n.664-445T=
ENST00000515652.5:c.572-445T=	ENSP00000425701.1:n.572-445T=
NM_001003841.2:c.664-445T=	NP_001003841.1:n.664-445T=
NM_001003841.3:c.664-445T= MANE Select	NP_001003841.1:n.664-445T=