Canonical Allele Identifier: CA338920550

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456150G>C (hg19) ; chr1:g.22129657G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129657G>C , CM000663.2:g.22129657G>C	GRCh38
NC_000001.10:g.22456150G>C , CM000663.1:g.22456150G>C	GRCh37
NC_000001.9:g.22328737G>C	NCBI36
NG_008974.1:g.18370C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.272C>G MANE Select	ENSP00000290167.5:p.Thr91Arg
ENST00000290167.10:c.272C>G	ENSP00000290167.5:p.Thr91Arg
ENST00000415567.1:c.195C>G
ENST00000441048.1:c.107C>G	ENSP00000388925.1:p.Thr36Arg
NM_030761.4:c.272C>G	NP_110388.2:p.Thr91Arg
XM_011541597.1:c.338C>G	XP_011539899.1:p.Thr113Arg
XM_011541598.1:c.107C>G	XP_011539900.1:p.Thr36Arg
XM_011541599.1:c.338C>G	XP_011539901.1:p.Thr113Arg
XM_011541597.2:c.338C>G	XP_011539899.1:p.Thr113Arg
XM_011541598.2:c.107C>G	XP_011539900.1:p.Thr36Arg
NM_030761.5:c.272C>G MANE Select	NP_110388.2:p.Thr91Arg