Canonical Allele Identifier: CA1522520777

Gene: SLC6A19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1213914T= , CM000667.2:g.1213914T=	GRCh38
NC_000005.9:g.1214029T= , CM000667.1:g.1214029T=	GRCh37
NC_000005.8:g.1267029T=	NCBI36
NG_008282.1:g.17320T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304460.11:c.775-39T= MANE Select	ENSP00000305302.10:n.775-39T=
ENST00000304460.10:c.775-39T=	ENSP00000305302.10:n.775-39T=
ENST00000515652.5:c.683-39T=	ENSP00000425701.1:n.683-39T=
NM_001003841.2:c.775-39T=	NP_001003841.1:n.775-39T=
NM_001003841.3:c.775-39T= MANE Select	NP_001003841.1:n.775-39T=