Canonical Allele Identifier: CA1158260807

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129711_22129712delinsAG , CM000663.2:g.22129711_22129712delinsAG	GRCh38
NC_000001.10:g.22456204_22456205delinsAG , CM000663.1:g.22456204_22456205delinsAG	GRCh37
NC_000001.9:g.22328791_22328792delinsAG	NCBI36
NG_008974.1:g.18315_18316delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.217_218delinsCT MANE Select	ENSP00000290167.5:p.Leu73=
ENST00000290167.10:c.217_218delinsCT	ENSP00000290167.5:p.Leu73=
ENST00000415567.1:c.140_141delinsCT
ENST00000441048.1:c.52_53delinsCT	ENSP00000388925.1:p.Leu18=
NM_030761.4:c.217_218delinsCT	NP_110388.2:p.Leu73=
XM_011541597.1:c.283_284delinsCT	XP_011539899.1:p.Leu95=
XM_011541598.1:c.52_53delinsCT	XP_011539900.1:p.Leu18=
XM_011541599.1:c.283_284delinsCT	XP_011539901.1:p.Leu95=
XM_011541597.2:c.283_284delinsCT	XP_011539899.1:p.Leu95=
XM_011541598.2:c.52_53delinsCT	XP_011539900.1:p.Leu18=
NM_030761.5:c.217_218delinsCT MANE Select	NP_110388.2:p.Leu73=