Canonical Allele Identifier: CA675507
Gene: WNT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2785066
ClinVar RCV Id: RCV003662623
dbSNP Id: rs757851512
ExAC: 1:22456294 C / T
gnomAD v3: 1-22129801-C-T
gnomAD v4: 1-22129801-C-T
MyVariant Identifiers: chr1:g.22456294C>T (hg19) chr1:g.22129801C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22129801C>T , CM000663.2:g.22129801C>T GRCh38
NC_000001.10:g.22456294C>T , CM000663.1:g.22456294C>T GRCh37
NC_000001.9:g.22328881C>T NCBI36
NG_008974.1:g.18226G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290167.11:c.128G>A MANE Select ENSP00000290167.5:p.Cys43Tyr
ENST00000290167.10:c.128G>A ENSP00000290167.5:p.Cys43Tyr
ENST00000415567.1:c.51G>A
ENST00000441048.1:c.-38G>A ENSP00000388925.1:n.-38G>A
NM_030761.4:c.128G>A NP_110388.2:p.Cys43Tyr
XM_011541597.1:c.194G>A XP_011539899.1:p.Cys65Tyr
XM_011541598.1:c.-38G>A XP_011539900.1:n.-38G>A
XM_011541599.1:c.194G>A XP_011539901.1:p.Cys65Tyr
XM_011541597.2:c.194G>A XP_011539899.1:p.Cys65Tyr
XM_011541598.2:c.-38G>A XP_011539900.1:n.-38G>A
NM_030761.5:c.128G>A MANE Select NP_110388.2:p.Cys43Tyr
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