Canonical Allele Identifier: CA1844935642

Gene: B4GALT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.33122237G= , CM000671.2:g.33122237G=	GRCh38
NC_000009.11:g.33122235G= , CM000671.1:g.33122235G=	GRCh37
NC_000009.10:g.33112235G=	NCBI36
NG_008919.1:g.50122C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379731.5:c.649-1631C= MANE Select	ENSP00000369055.4:n.649-1631C=
ENST00000379731.4:c.649-1631C=	ENSP00000369055.4:n.649-1631C=
ENST00000535206.5:c.648+12952C=	ENSP00000440341.1:n.648+12952C=
NM_001497.3:c.649-1631C=	NP_001488.2:n.649-1631C=
XM_005251440.3:c.649-1631C=	XP_005251497.1:n.649-1631C=
XM_005251440.5:c.649-1631C=	XP_005251497.1:n.649-1631C=
NM_001378495.1:c.610-1631C=	NP_001365424.1:n.610-1631C=
NM_001378496.1:c.649-1631C=	NP_001365425.1:n.649-1631C=
NM_001378497.1:c.648+12952C=	NP_001365426.1:n.648+12952C=
NM_001497.4:c.649-1631C= MANE Select	NP_001488.2:n.649-1631C=