Canonical Allele Identifier: CA1603685353

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608937G= , CM000667.2:g.177608937G=	GRCh38
NC_000005.9:g.177035938G= , CM000667.1:g.177035938G=	GRCh37
NC_000005.8:g.176968544G=	NCBI36
NG_015977.1:g.13820G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.751G= MANE Select	ENSP00000029410.5:p.Gly251=
ENST00000029410.9:c.751G=	ENSP00000029410.5:p.Gly251=
ENST00000505145.1:n.1849G=
ENST00000505433.5:c.*257G=	ENSP00000425591.1:n.*257G=
ENST00000515353.1:n.1573G=
NM_007255.2:c.751G=	NP_009186.1:p.Gly251=
XM_005265805.2:c.409G=	XP_005265862.1:p.Gly137=
XM_006714816.2:c.271G=	XP_006714879.1:p.Gly91=
XM_011534421.1:c.409G=	XP_011532723.1:p.Gly137=
XM_006714816.4:c.271G=	XP_006714879.1:p.Gly91=
XM_017008999.2:c.409G=	XP_016864488.1:p.Gly137=
NM_007255.3:c.751G= MANE Select	NP_009186.1:p.Gly251=