Canonical Allele Identifier: CA338920906

Gene: WNT4

Linked Data

• MyVariant Identifiers: chr1:g.22456188G>C (hg19) ; chr1:g.22129695G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129695G>C , CM000663.2:g.22129695G>C	GRCh38
NC_000001.10:g.22456188G>C , CM000663.1:g.22456188G>C	GRCh37
NC_000001.9:g.22328775G>C	NCBI36
NG_008974.1:g.18332C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000290167.11:c.234C>G MANE Select	ENSP00000290167.5:p.Cys78Trp
ENST00000290167.10:c.234C>G	ENSP00000290167.5:p.Cys78Trp
ENST00000415567.1:c.157C>G
ENST00000441048.1:c.69C>G	ENSP00000388925.1:p.Cys23Trp
NM_030761.4:c.234C>G	NP_110388.2:p.Cys78Trp
XM_011541597.1:c.300C>G	XP_011539899.1:p.Cys100Trp
XM_011541598.1:c.69C>G	XP_011539900.1:p.Cys23Trp
XM_011541599.1:c.300C>G	XP_011539901.1:p.Cys100Trp
XM_011541597.2:c.300C>G	XP_011539899.1:p.Cys100Trp
XM_011541598.2:c.69C>G	XP_011539900.1:p.Cys23Trp
NM_030761.5:c.234C>G MANE Select	NP_110388.2:p.Cys78Trp