Canonical Allele Identifier: CA1603685577

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608991A= , CM000667.2:g.177608991A=	GRCh38
NC_000005.9:g.177035992A= , CM000667.1:g.177035992A=	GRCh37
NC_000005.8:g.176968598A=	NCBI36
NG_015977.1:g.13874A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.805A= MANE Select	ENSP00000029410.5:p.Lys269=
ENST00000029410.9:c.805A=	ENSP00000029410.5:p.Lys269=
ENST00000505145.1:n.1903A=
ENST00000505433.5:c.*311A=	ENSP00000425591.1:n.*311A=
ENST00000515353.1:n.1627A=
NM_007255.2:c.805A=	NP_009186.1:p.Lys269=
XM_005265805.2:c.463A=	XP_005265862.1:p.Lys155=
XM_006714816.2:c.325A=	XP_006714879.1:p.Lys109=
XM_011534421.1:c.463A=	XP_011532723.1:p.Lys155=
XM_006714816.4:c.325A=	XP_006714879.1:p.Lys109=
XM_017008999.2:c.463A=	XP_016864488.1:p.Lys155=
NM_007255.3:c.805A= MANE Select	NP_009186.1:p.Lys269=