Canonical Allele Identifier: CA1158260852

Gene: WNT4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129834G= , CM000663.2:g.22129834G=	GRCh38
NC_000001.10:g.22456327G= , CM000663.1:g.22456327G=	GRCh37
NC_000001.9:g.22328914G=	NCBI36
NG_008974.1:g.18193C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.95C= MANE Select	ENSP00000290167.5:p.Ser32=
ENST00000290167.10:c.95C=	ENSP00000290167.5:p.Ser32=
ENST00000415567.1:c.18C=
ENST00000441048.1:c.-71C=	ENSP00000388925.1:n.-71C=
NM_030761.4:c.95C=	NP_110388.2:p.Ser32=
XM_011541597.1:c.161C=	XP_011539899.1:p.Ser54=
XM_011541598.1:c.-71C=	XP_011539900.1:n.-71C=
XM_011541599.1:c.161C=	XP_011539901.1:p.Ser54=
XM_011541597.2:c.161C=	XP_011539899.1:p.Ser54=
XM_011541598.2:c.-71C=	XP_011539900.1:n.-71C=
NM_030761.5:c.95C= MANE Select	NP_110388.2:p.Ser32=