Canonical Allele Identifier: CA1603675525

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604462G= , CM000667.2:g.177604462G=	GRCh38
NC_000005.9:g.177031463G= , CM000667.1:g.177031463G=	GRCh37
NC_000005.8:g.176964069G=	NCBI36
NG_015977.1:g.9345G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.334G= MANE Select	ENSP00000029410.5:p.Val112=
ENST00000029410.9:c.334G=	ENSP00000029410.5:p.Val112=
ENST00000502420.1:n.313G=
ENST00000505433.5:c.334G=	ENSP00000425591.1:p.Val112=
ENST00000505468.1:c.-9G=	ENSP00000420886.1:n.-9G=
ENST00000507061.1:c.151G=	ENSP00000423868.1:p.Val51=
ENST00000510761.1:c.-9G=	ENSP00000423438.1:n.-9G=
NM_007255.2:c.334G=	NP_009186.1:p.Val112=
XM_005265805.2:c.-9G=	XP_005265862.1:n.-9G=
XM_006714816.2:c.-166G=	XP_006714879.1:n.-166G=
XM_011534421.1:c.-9G=	XP_011532723.1:n.-9G=
XM_006714816.4:c.-166G=	XP_006714879.1:n.-166G=
XM_017008999.2:c.-9G=	XP_016864488.1:n.-9G=
NM_007255.3:c.334G= MANE Select	NP_009186.1:p.Val112=