Canonical Allele Identifier: CA1158260800

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129692C= , CM000663.2:g.22129692C=	GRCh38
NC_000001.10:g.22456185C= , CM000663.1:g.22456185C=	GRCh37
NC_000001.9:g.22328772C=	NCBI36
NG_008974.1:g.18335G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000290167.11:c.237G= MANE Select	ENSP00000290167.5:p.Gln79=
ENST00000290167.10:c.237G=	ENSP00000290167.5:p.Gln79=
ENST00000415567.1:c.160G=
ENST00000441048.1:c.72G=	ENSP00000388925.1:p.Gln24=
NM_030761.4:c.237G=	NP_110388.2:p.Gln79=
XM_011541597.1:c.303G=	XP_011539899.1:p.Gln101=
XM_011541598.1:c.72G=	XP_011539900.1:p.Gln24=
XM_011541599.1:c.303G=	XP_011539901.1:p.Gln101=
XM_011541597.2:c.303G=	XP_011539899.1:p.Gln101=
XM_011541598.2:c.72G=	XP_011539900.1:p.Gln24=
NM_030761.5:c.237G= MANE Select	NP_110388.2:p.Gln79=