Canonical Allele Identifier: CA1158260856

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129850A= , CM000663.2:g.22129850A=	GRCh38
NC_000001.10:g.22456343A= , CM000663.1:g.22456343A=	GRCh37
NC_000001.9:g.22328930A=	NCBI36
NG_008974.1:g.18177T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.79T= MANE Select	ENSP00000290167.5:p.Tyr27=
ENST00000290167.10:c.79T=	ENSP00000290167.5:p.Tyr27=
ENST00000415567.1:c.2T=
ENST00000441048.1:c.-87T=	ENSP00000388925.1:n.-87T=
NM_030761.4:c.79T=	NP_110388.2:p.Tyr27=
XM_011541597.1:c.145T=	XP_011539899.1:p.Tyr49=
XM_011541598.1:c.-87T=	XP_011539900.1:n.-87T=
XM_011541599.1:c.145T=	XP_011539901.1:p.Tyr49=
XM_011541597.2:c.145T=	XP_011539899.1:p.Tyr49=
XM_011541598.2:c.-87T=	XP_011539900.1:n.-87T=
NM_030761.5:c.79T= MANE Select	NP_110388.2:p.Tyr27=