Canonical Allele Identifier: CA1139997346

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22141722C= , CM000663.2:g.22141722C=	GRCh38
NC_000001.10:g.22468215C= , CM000663.1:g.22468215C=	GRCh37
NC_000001.9:g.22340802C=	NCBI36
NG_008974.1:g.6305G=

Transcript Alleles

HGVS	Amino-acid Change
NM_030761.5:c.77+1124G= MANE Select	NP_110388.2:n.77+1124G=
ENST00000290167.11:c.77+1124G= MANE Select	ENSP00000290167.5:n.77+1124G=
NM_030761.4:c.77+1124G=	NP_110388.2:n.77+1124G=
ENST00000290167.10:c.77+1124G=	ENSP00000290167.5:n.77+1124G=
ENST00000441048.1:c.-89+2010G=	ENSP00000388925.1:n.-89+2010G=
XM_011541597.1:c.-922G=	XP_011539899.1:n.-922G=
XM_011541597.2:c.-922G=	XP_011539899.1:n.-922G=
XM_011541598.1:c.-89+2010G=	XP_011539900.1:n.-89+2010G=
XM_011541598.2:c.-89+2010G=	XP_011539900.1:n.-89+2010G=
XR_947050.1:n.53+717C=