Canonical Allele Identifier: CA1140640533
Gene: WNT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22143914C= , CM000663.2:g.22143914C= GRCh38
NC_000001.10:g.22470407C= , CM000663.1:g.22470407C= GRCh37
NC_000001.9:g.22342994C= NCBI36
NG_008974.1:g.4113G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000441048.1:c.-271G= ENSP00000388925.1:n.-271G=
XM_011541598.1:c.-271G= XP_011539900.1:n.-271G=
XR_947049.1:n.82+1010C=
XR_947050.1:n.53+2909C=
XR_947051.1:n.47+923C=
XR_947053.1:n.82+1010C=
XR_947054.1:n.82+1010C=
XR_947055.1:n.82+1010C=
XM_011541598.2:c.-271G= XP_011539900.1:n.-271G=
XR_001737923.1:n.52+923C=
XR_001737924.1:n.52+923C=
XR_001737925.1:n.52+923C=
XR_947051.2:n.52+923C=