Canonical Allele Identifier: CA1158260857

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129851C= , CM000663.2:g.22129851C=	GRCh38
NC_000001.10:g.22456344C= , CM000663.1:g.22456344C=	GRCh37
NC_000001.9:g.22328931C=	NCBI36
NG_008974.1:g.18176G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.78G= MANE Select	ENSP00000290167.5:p.Leu26=
ENST00000290167.10:c.78G=	ENSP00000290167.5:p.Leu26=
ENST00000415567.1:c.1G=
ENST00000441048.1:c.-88G=	ENSP00000388925.1:n.-88G=
NM_030761.4:c.78G=	NP_110388.2:p.Leu26=
XM_011541597.1:c.144G=	XP_011539899.1:p.Arg48=
XM_011541598.1:c.-88G=	XP_011539900.1:n.-88G=
XM_011541599.1:c.144G=	XP_011539901.1:p.Arg48=
XM_011541597.2:c.144G=	XP_011539899.1:p.Arg48=
XM_011541598.2:c.-88G=	XP_011539900.1:n.-88G=
NM_030761.5:c.78G= MANE Select	NP_110388.2:p.Leu26=