Canonical Allele Identifier: CA416559178

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456175G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129682G>T , CM000663.2:g.22129682G>T	GRCh38
NC_000001.10:g.22456175G>T , CM000663.1:g.22456175G>T	GRCh37
NC_000001.9:g.22328762G>T	NCBI36
NG_008974.1:g.18345C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000290167.11:c.247C>A MANE Select	ENSP00000290167.5:p.Arg83=
ENST00000290167.10:c.247C>A	ENSP00000290167.5:p.Arg83=
ENST00000415567.1:c.170C>A
ENST00000441048.1:c.82C>A	ENSP00000388925.1:p.Arg28=
NM_030761.4:c.247C>A	NP_110388.2:p.Arg83=
XM_011541597.1:c.313C>A	XP_011539899.1:p.Arg105=
XM_011541598.1:c.82C>A	XP_011539900.1:p.Arg28=
XM_011541599.1:c.313C>A	XP_011539901.1:p.Arg105=
XM_011541597.2:c.313C>A	XP_011539899.1:p.Arg105=
XM_011541598.2:c.82C>A	XP_011539900.1:p.Arg28=
NM_030761.5:c.247C>A MANE Select	NP_110388.2:p.Arg83=