Canonical Allele Identifier: CA1603730262

Gene: B4GALT7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604193C= , CM000667.2:g.177604193C=	GRCh38
NC_000005.9:g.177031194C= , CM000667.1:g.177031194C=	GRCh37
NC_000005.8:g.176963800C=	NCBI36
NG_015977.1:g.9076C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.65C= MANE Select	ENSP00000029410.5:p.Ser22=
ENST00000029410.9:c.65C=	ENSP00000029410.5:p.Ser22=
ENST00000502420.1:n.130-86C=
ENST00000505433.5:c.65C=	ENSP00000425591.1:p.Ser22=
ENST00000505468.1:c.-278C=	ENSP00000420886.1:n.-278C=
ENST00000510761.1:c.-278C=	ENSP00000423438.1:n.-278C=
NM_007255.2:c.65C=	NP_009186.1:p.Ser22=
XM_005265805.2:c.-278C=	XP_005265862.1:n.-278C=
XM_006714816.2:c.-435C=	XP_006714879.1:n.-435C=
XM_011534421.1:c.-278C=	XP_011532723.1:n.-278C=
XM_006714816.4:c.-435C=	XP_006714879.1:n.-435C=
XM_017008999.2:c.-278C=	XP_016864488.1:n.-278C=
NM_007255.3:c.65C= MANE Select	NP_009186.1:p.Ser22=