Canonical Allele Identifier: CA1603730212

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604110C= , CM000667.2:g.177604110C=	GRCh38
NC_000005.9:g.177031111C= , CM000667.1:g.177031111C=	GRCh37
NC_000005.8:g.176963717C=	NCBI36
NG_015977.1:g.8993C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.51-69C= MANE Select	ENSP00000029410.5:n.51-69C=
ENST00000029410.9:c.51-69C=	ENSP00000029410.5:n.51-69C=
ENST00000502420.1:n.130-169C=
ENST00000505433.5:c.51-69C=	ENSP00000425591.1:n.51-69C=
ENST00000505468.1:c.-361C=	ENSP00000420886.1:n.-361C=
ENST00000510761.1:c.-292-69C=	ENSP00000423438.1:n.-292-69C=
NM_007255.2:c.51-69C=	NP_009186.1:n.51-69C=
XM_005265805.2:c.-292-69C=	XP_005265862.1:n.-292-69C=
XM_006714816.2:c.-449-69C=	XP_006714879.1:n.-449-69C=
XM_011534421.1:c.-292-69C=	XP_011532723.1:n.-292-69C=
XM_006714816.4:c.-449-69C=	XP_006714879.1:n.-449-69C=
XM_017008999.2:c.-292-69C=	XP_016864488.1:n.-292-69C=
NM_007255.3:c.51-69C= MANE Select	NP_009186.1:n.51-69C=