Canonical Allele Identifier: CA1148568505

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129812C= , CM000663.2:g.22129812C=	GRCh38
NC_000001.10:g.22456305C= , CM000663.1:g.22456305C=	GRCh37
NC_000001.9:g.22328892C=	NCBI36
NG_008974.1:g.18215G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.117G= MANE Select	ENSP00000290167.5:p.Glu39=
ENST00000290167.10:c.117G=	ENSP00000290167.5:p.Glu39=
ENST00000415567.1:c.40G=
ENST00000441048.1:c.-49G=	ENSP00000388925.1:n.-49G=
NM_030761.4:c.117G=	NP_110388.2:p.Glu39=
XM_011541597.1:c.183G=	XP_011539899.1:p.Glu61=
XM_011541598.1:c.-49G=	XP_011539900.1:n.-49G=
XM_011541599.1:c.183G=	XP_011539901.1:p.Glu61=
XM_011541597.2:c.183G=	XP_011539899.1:p.Glu61=
XM_011541598.2:c.-49G=	XP_011539900.1:n.-49G=
NM_030761.5:c.117G= MANE Select	NP_110388.2:p.Glu39=