Canonical Allele Identifier: CA1158260770

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129585T= , CM000663.2:g.22129585T=	GRCh38
NC_000001.10:g.22456078T= , CM000663.1:g.22456078T=	GRCh37
NC_000001.9:g.22328665T=	NCBI36
NG_008974.1:g.18442A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.313+31A= MANE Select	ENSP00000290167.5:n.313+31A=
ENST00000290167.10:c.313+31A=	ENSP00000290167.5:n.313+31A=
ENST00000415567.1:c.236+31A=
ENST00000441048.1:c.148+31A=	ENSP00000388925.1:n.148+31A=
NM_030761.4:c.313+31A=	NP_110388.2:n.313+31A=
XM_011541597.1:c.379+31A=	XP_011539899.1:n.379+31A=
XM_011541598.1:c.148+31A=	XP_011539900.1:n.148+31A=
XM_011541599.1:c.379+31A=	XP_011539901.1:n.379+31A=
XM_011541597.2:c.379+31A=	XP_011539899.1:n.379+31A=
XM_011541598.2:c.148+31A=	XP_011539900.1:n.148+31A=
NM_030761.5:c.313+31A= MANE Select	NP_110388.2:n.313+31A=