Canonical Allele Identifier: CA1603675398

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604441T= , CM000667.2:g.177604441T=	GRCh38
NC_000005.9:g.177031442T= , CM000667.1:g.177031442T=	GRCh37
NC_000005.8:g.176964048T=	NCBI36
NG_015977.1:g.9324T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.313T= MANE Select	ENSP00000029410.5:p.Phe105=
ENST00000029410.9:c.313T=	ENSP00000029410.5:p.Phe105=
ENST00000502420.1:n.292T=
ENST00000505433.5:c.313T=	ENSP00000425591.1:p.Phe105=
ENST00000505468.1:c.-30T=	ENSP00000420886.1:n.-30T=
ENST00000507061.1:c.130T=	ENSP00000423868.1:p.Phe44=
ENST00000510761.1:c.-30T=	ENSP00000423438.1:n.-30T=
NM_007255.2:c.313T=	NP_009186.1:p.Phe105=
XM_005265805.2:c.-30T=	XP_005265862.1:n.-30T=
XM_006714816.2:c.-187T=	XP_006714879.1:n.-187T=
XM_011534421.1:c.-30T=	XP_011532723.1:n.-30T=
XM_006714816.4:c.-187T=	XP_006714879.1:n.-187T=
XM_017008999.2:c.-30T=	XP_016864488.1:n.-30T=
NM_007255.3:c.313T= MANE Select	NP_009186.1:p.Phe105=