Canonical Allele Identifier: CA1603684872

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608733C= , CM000667.2:g.177608733C=	GRCh38
NC_000005.9:g.177035734C= , CM000667.1:g.177035734C=	GRCh37
NC_000005.8:g.176968340C=	NCBI36
NG_015977.1:g.13616C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.723+111C= MANE Select	ENSP00000029410.5:n.723+111C=
ENST00000029410.9:c.723+111C=	ENSP00000029410.5:n.723+111C=
ENST00000505145.1:n.1821+111C=
ENST00000505433.5:c.*229+111C=	ENSP00000425591.1:n.*229+111C=
ENST00000515353.1:n.1369C=
NM_007255.2:c.723+111C=	NP_009186.1:n.723+111C=
XM_005265805.2:c.381+111C=	XP_005265862.1:n.381+111C=
XM_006714816.2:c.243+111C=	XP_006714879.1:n.243+111C=
XM_011534421.1:c.381+111C=	XP_011532723.1:n.381+111C=
XM_006714816.4:c.243+111C=	XP_006714879.1:n.243+111C=
XM_017008999.2:c.381+111C=	XP_016864488.1:n.381+111C=
NM_007255.3:c.723+111C= MANE Select	NP_009186.1:n.723+111C=