Canonical Allele Identifier: CA1977847677

Gene: B3GAT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62616590A= , CM000673.2:g.62616590A=	GRCh38
NC_000011.9:g.62384062A= , CM000673.1:g.62384062A=	GRCh37
NC_000011.8:g.62140638A=	NCBI36
NG_009845.1:g.8850A=
NG_031863.1:g.10586T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265471.10:c.825T= MANE Select	ENSP00000265471.5:p.Ala275=
ENST00000265471.9:c.825T=	ENSP00000265471.5:p.Ala275=
ENST00000531383.5:c.825T=	ENSP00000431359.1:p.Ala275=
ENST00000532585.5:c.*947T=	ENSP00000432604.1:n.*947T=
ENST00000534026.5:c.825T=	ENSP00000432474.1:p.Ala275=
NM_001288721.1:c.804T=	NP_001275650.1:p.Ala268=
NM_001288722.1:c.825T=	NP_001275651.1:p.Ala275=
NM_001288723.1:c.825T=	NP_001275652.1:p.Ala275=
NM_012200.3:c.825T=	NP_036332.2:p.Ala275=
NR_109991.1:n.1043T=
XM_011544936.1:c.804T=	XP_011543238.1:p.Ala268=
NM_012200.4:c.825T= MANE Select	NP_036332.2:p.Ala275=
NM_001288721.2:c.804T=	NP_001275650.1:p.Ala268=
NM_001288722.2:c.825T=	NP_001275651.1:p.Ala275=
NM_001288723.2:c.825T=	NP_001275652.1:p.Ala275=
NR_109991.2:n.854T=