Canonical Allele Identifier: CA416559305

Gene: WNT4

Linked Data

• ClinVar Variation Id: 3061199
• ClinVar RCV Id: RCV003982711
• dbSNP Id: rs779327911
• gnomAD v4: 1-22129803-C-G
• COSMIC: COSM6124911 ; COSM6124912
• MyVariant Identifiers: chr1:g.22456296C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22129803C>G , CM000663.2:g.22129803C>G	GRCh38
NC_000001.10:g.22456296C>G , CM000663.1:g.22456296C>G	GRCh37
NC_000001.9:g.22328883C>G	NCBI36
NG_008974.1:g.18224G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290167.11:c.126G>C MANE Select	ENSP00000290167.5:p.Thr42=
ENST00000290167.10:c.126G>C	ENSP00000290167.5:p.Thr42=
ENST00000415567.1:c.49G>C
ENST00000441048.1:c.-40G>C	ENSP00000388925.1:n.-40G>C
NM_030761.4:c.126G>C	NP_110388.2:p.Thr42=
XM_011541597.1:c.192G>C	XP_011539899.1:p.Thr64=
XM_011541598.1:c.-40G>C	XP_011539900.1:n.-40G>C
XM_011541599.1:c.192G>C	XP_011539901.1:p.Thr64=
XM_011541597.2:c.192G>C	XP_011539899.1:p.Thr64=
XM_011541598.2:c.-40G>C	XP_011539900.1:n.-40G>C
NM_030761.5:c.126G>C MANE Select	NP_110388.2:p.Thr42=