Canonical Allele Identifier: CA1603684655

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608621A= , CM000667.2:g.177608621A=	GRCh38
NC_000005.9:g.177035622A= , CM000667.1:g.177035622A=	GRCh37
NC_000005.8:g.176968228A=	NCBI36
NG_015977.1:g.13504A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.722A= MANE Select	ENSP00000029410.5:p.Gln241=
ENST00000029410.9:c.722A=	ENSP00000029410.5:p.Gln241=
ENST00000505145.1:n.1820A=
ENST00000505433.5:c.*228A=	ENSP00000425591.1:n.*228A=
ENST00000515353.1:n.1257A=
NM_007255.2:c.722A=	NP_009186.1:p.Gln241=
XM_005265805.2:c.380A=	XP_005265862.1:p.Gln127=
XM_006714816.2:c.242A=	XP_006714879.1:p.Gln81=
XM_011534421.1:c.380A=	XP_011532723.1:p.Gln127=
XM_006714816.4:c.242A=	XP_006714879.1:p.Gln81=
XM_017008999.2:c.380A=	XP_016864488.1:p.Gln127=
NM_007255.3:c.722A= MANE Select	NP_009186.1:p.Gln241=