Canonical Allele Identifier: CA1603675598

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604483C= , CM000667.2:g.177604483C=	GRCh38
NC_000005.9:g.177031484C= , CM000667.1:g.177031484C=	GRCh37
NC_000005.8:g.176964090C=	NCBI36
NG_015977.1:g.9366C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.355C= MANE Select	ENSP00000029410.5:p.Leu119=
ENST00000029410.9:c.355C=	ENSP00000029410.5:p.Leu119=
ENST00000502420.1:n.334C=
ENST00000505433.5:c.355C=	ENSP00000425591.1:p.Leu119=
ENST00000505468.1:c.13C=	ENSP00000420886.1:p.Leu5=
ENST00000507061.1:c.172C=	ENSP00000423868.1:p.Leu58=
ENST00000510761.1:c.13C=	ENSP00000423438.1:p.Leu5=
NM_007255.2:c.355C=	NP_009186.1:p.Leu119=
XM_005265805.2:c.13C=	XP_005265862.1:p.Leu5=
XM_006714816.2:c.-145C=	XP_006714879.1:n.-145C=
XM_011534421.1:c.13C=	XP_011532723.1:p.Leu5=
XM_006714816.4:c.-145C=	XP_006714879.1:n.-145C=
XM_017008999.2:c.13C=	XP_016864488.1:p.Leu5=
NM_007255.3:c.355C= MANE Select	NP_009186.1:p.Leu119=