Canonical Allele Identifier: CA1305690623

Gene: B3GALT1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.167789531A= , CM000664.2:g.167789531A=	GRCh38
NC_000002.11:g.168646041A= , CM000664.1:g.168646041A=	GRCh37
NC_000002.10:g.168354287A=	NCBI36
NG_050644.1:g.501471A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392690.4:c.-351-29141A= MANE Select	ENSP00000376456.2:n.-351-29141A=
XM_005246931.2:c.-351-29141A=	XP_005246988.1:n.-351-29141A=
XM_006712819.2:c.-351-29141A=	XP_006712882.1:n.-351-29141A=
XM_011512084.1:c.-351-29141A=	XP_011510386.1:n.-351-29141A=
XM_011512085.1:c.-367-29141A=	XP_011510387.1:n.-367-29141A=
XM_005246931.3:c.-351-29141A=	XP_005246988.1:n.-351-29141A=
XM_006712819.3:c.-351-29141A=	XP_006712882.1:n.-351-29141A=
XM_011512085.2:c.-367-29141A=	XP_011510387.1:n.-367-29141A=
NM_020981.4:c.-351-29141A= MANE Select	NP_066191.1:n.-351-29141A=