Canonical Allele Identifier: CA1603685626

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608999C= , CM000667.2:g.177608999C=	GRCh38
NC_000005.9:g.177036000C= , CM000667.1:g.177036000C=	GRCh37
NC_000005.8:g.176968606C=	NCBI36
NG_015977.1:g.13882C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.813C= MANE Select	ENSP00000029410.5:p.Ile271=
ENST00000029410.9:c.813C=	ENSP00000029410.5:p.Ile271=
ENST00000505145.1:n.1911C=
ENST00000505433.5:c.*319C=	ENSP00000425591.1:n.*319C=
ENST00000515353.1:n.1635C=
NM_007255.2:c.813C=	NP_009186.1:p.Ile271=
XM_005265805.2:c.471C=	XP_005265862.1:p.Ile157=
XM_006714816.2:c.333C=	XP_006714879.1:p.Ile111=
XM_011534421.1:c.471C=	XP_011532723.1:p.Ile157=
XM_006714816.4:c.333C=	XP_006714879.1:p.Ile111=
XM_017008999.2:c.471C=	XP_016864488.1:p.Ile157=
NM_007255.3:c.813C= MANE Select	NP_009186.1:p.Ile271=