Canonical Allele Identifier: CA1158260808

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129714T= , CM000663.2:g.22129714T=	GRCh38
NC_000001.10:g.22456207T= , CM000663.1:g.22456207T=	GRCh37
NC_000001.9:g.22328794T=	NCBI36
NG_008974.1:g.18313A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.215A= MANE Select	ENSP00000290167.5:p.Gln72=
ENST00000290167.10:c.215A=	ENSP00000290167.5:p.Gln72=
ENST00000415567.1:c.138A=
ENST00000441048.1:c.50A=	ENSP00000388925.1:p.Gln17=
NM_030761.4:c.215A=	NP_110388.2:p.Gln72=
XM_011541597.1:c.281A=	XP_011539899.1:p.Gln94=
XM_011541598.1:c.50A=	XP_011539900.1:p.Gln17=
XM_011541599.1:c.281A=	XP_011539901.1:p.Gln94=
XM_011541597.2:c.281A=	XP_011539899.1:p.Gln94=
XM_011541598.2:c.50A=	XP_011539900.1:p.Gln17=
NM_030761.5:c.215A= MANE Select	NP_110388.2:p.Gln72=