Canonical Allele Identifier: CA1158256863

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22120369G= , CM000663.2:g.22120369G=	GRCh38
NC_000001.10:g.22446862G= , CM000663.1:g.22446862G=	GRCh37
NC_000001.9:g.22319449G=	NCBI36
NG_008974.1:g.27658C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000290167.11:c.737C= MANE Select	ENSP00000290167.5:p.Pro246=
ENST00000290167.10:c.737C=	ENSP00000290167.5:p.Pro246=
NM_030761.4:c.737C=	NP_110388.2:p.Pro246=
XM_011541597.1:c.803C=	XP_011539899.1:p.Pro268=
XM_011541598.1:c.572C=	XP_011539900.1:p.Pro191=
XM_011541597.2:c.803C=	XP_011539899.1:p.Pro268=
XM_011541598.2:c.572C=	XP_011539900.1:p.Pro191=
NM_030761.5:c.737C= MANE Select	NP_110388.2:p.Pro246=