Canonical Allele Identifier: CA351790
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 222890
ClinVar RCV Id: RCV000208133 RCV003223623
dbSNP Id: rs869025561
COSMIC: COSM5945687
MyVariant Identifiers: chr11:g.32414301C>A (hg19) chr11:g.32392755C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392755C>A , CM000673.2:g.32392755C>A GRCh38
NC_000011.9:g.32414301C>A , CM000673.1:g.32414301C>A GRCh37
NC_000011.8:g.32370877C>A NCBI36
NG_009272.1:g.47787G>T , LRG_525:g.47787G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.1214G>T ENSP00000331327.5:p.Gly405Val
ENST00000379077.9:c.*449G>T ENSP00000368368.5:n.*449G>T
ENST00000379079.8:c.614G>T ENSP00000368370.2:p.Gly205Val
ENST00000448076.9:c.1265G>T ENSP00000413452.5:p.Gly422Val
ENST00000452863.10:c.1265G>T MANE Select ENSP00000415516.5:p.Gly422Val
ENST00000526685.2:n.719G>T
ENST00000639563.3:c.1214G>T ENSP00000492269.3:p.Gly405Val
ENST00000639907.2:n.408G>T
ENST00000640146.2:c.590G>T ENSP00000491984.2:p.Gly197Val
ENST00000650745.1:n.474G>T
ENST00000650861.1:n.1846G>T
ENST00000651459.1:c.36G>T
ENST00000651533.1:n.311G>T
ENST00000651668.1:n.202G>T
ENST00000651794.1:n.1108G>T
ENST00000651819.1:n.190G>T
ENST00000652579.1:n.525G>T
ENST00000652724.1:n.455G>T
ENST00000332351.7:c.1250G>T ENSP00000331327.3:p.Gly417Val
ENST00000379077.7:c.*449G>T ENSP00000368368.3:n.*449G>T
ENST00000379079.6:c.614G>T ENSP00000368370.2:p.Gly205Val
ENST00000448076.7:c.1250G>T ENSP00000413452.3:p.Gly417Val
ENST00000452863.7:c.1199G>T ENSP00000415516.3:p.Gly400Val
ENST00000527882.5:c.321-691G>T
ENST00000530998.5:c.563G>T ENSP00000435307.1:p.Gly188Val
NM_000378.4:c.1199G>T NP_000369.3:p.Gly400Val
NM_001198551.1:c.614G>T , LRG_525t2:c.614G>T NP_001185480.1:p.Gly205Val
NM_001198552.1:c.563G>T NP_001185481.1:p.Gly188Val
NM_024424.3:c.1250G>T NP_077742.2:p.Gly417Val
NM_024426.4:c.1250G>T NP_077744.3:p.Gly417Val
NM_000378.5:c.1214G>T NP_000369.4:p.Gly405Val
NM_024424.4:c.1265G>T NP_077742.3:p.Gly422Val
NM_024426.5:c.1265G>T NP_077744.4:p.Gly422Val
NM_001367854.1:c.77G>T NP_001354783.1:p.Gly26Val
NR_160306.1:n.1597G>T
NM_000378.6:c.1214G>T NP_000369.4:p.Gly405Val
NM_001198552.2:c.563G>T NP_001185481.1:p.Gly188Val
NM_024424.5:c.1265G>T NP_077742.3:p.Gly422Val
NM_024426.6:c.1265G>T MANE Select NP_077744.4:p.Gly422Val
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