Canonical Allele Identifier: CA1522520188

Gene: SLC6A19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1213451C= , CM000667.2:g.1213451C=	GRCh38
NC_000005.9:g.1213566C= , CM000667.1:g.1213566C=	GRCh37
NC_000005.8:g.1266566C=	NCBI36
NG_008282.1:g.16857C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304460.11:c.664-12C= MANE Select	ENSP00000305302.10:n.664-12C=
ENST00000304460.10:c.664-12C=	ENSP00000305302.10:n.664-12C=
ENST00000515652.5:c.572-12C=	ENSP00000425701.1:n.572-12C=
NM_001003841.2:c.664-12C=	NP_001003841.1:n.664-12C=
NM_001003841.3:c.664-12C= MANE Select	NP_001003841.1:n.664-12C=