Canonical Allele Identifier: CA1603675818

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604539C= , CM000667.2:g.177604539C=	GRCh38
NC_000005.9:g.177031540C= , CM000667.1:g.177031540C=	GRCh37
NC_000005.8:g.176964146C=	NCBI36
NG_015977.1:g.9422C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.411C= MANE Select	ENSP00000029410.5:p.Phe137=
ENST00000029410.9:c.411C=	ENSP00000029410.5:p.Phe137=
ENST00000502420.1:n.390C=
ENST00000505433.5:c.411C=	ENSP00000425591.1:p.Phe137=
ENST00000505468.1:c.69C=	ENSP00000420886.1:p.Phe23=
ENST00000507061.1:c.228C=	ENSP00000423868.1:p.Phe76=
ENST00000510761.1:c.69C=	ENSP00000423438.1:p.Phe23=
NM_007255.2:c.411C=	NP_009186.1:p.Phe137=
XM_005265805.2:c.69C=	XP_005265862.1:p.Phe23=
XM_006714816.2:c.-89C=	XP_006714879.1:n.-89C=
XM_011534421.1:c.69C=	XP_011532723.1:p.Phe23=
XM_006714816.4:c.-89C=	XP_006714879.1:n.-89C=
XM_017008999.2:c.69C=	XP_016864488.1:p.Phe23=
NM_007255.3:c.411C= MANE Select	NP_009186.1:p.Phe137=