Canonical Allele Identifier: CA1522520484

Gene: SLC6A19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1213651A= , CM000667.2:g.1213651A=	GRCh38
NC_000005.9:g.1213766A= , CM000667.1:g.1213766A=	GRCh37
NC_000005.8:g.1266766A=	NCBI36
NG_008282.1:g.17057A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304460.11:c.774+78A= MANE Select	ENSP00000305302.10:n.774+78A=
ENST00000304460.10:c.774+78A=	ENSP00000305302.10:n.774+78A=
ENST00000515652.5:c.682+78A=	ENSP00000425701.1:n.682+78A=
NM_001003841.2:c.774+78A=	NP_001003841.1:n.774+78A=
NM_001003841.3:c.774+78A= MANE Select	NP_001003841.1:n.774+78A=