Canonical Allele Identifier: CA016316
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3504
ClinVar RCV Id: RCV000003679
dbSNP Id: rs28941779

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392026A>G , CM000673.2:g.32392026A>G GRCh38
NC_000011.9:g.32413572A>G , CM000673.1:g.32413572A>G GRCh37
NC_000011.8:g.32370148A>G NCBI36
NG_009272.1:g.48516T>C , LRG_525:g.48516T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1342T>C ENSP00000331327.5:p.Phe448Leu
ENST00000379077.9:c.*577T>C ENSP00000368368.5:n.*577T>C
ENST00000379079.8:c.742T>C ENSP00000368370.2:p.Phe248Leu
ENST00000448076.9:c.1393T>C ENSP00000413452.5:p.Phe465Leu
ENST00000452863.10:c.1393T>C MANE Select ENSP00000415516.5:p.Phe465Leu
ENST00000526685.2:n.847T>C
ENST00000639563.3:c.1342T>C ENSP00000492269.3:p.Phe448Leu
ENST00000639907.2:n.536T>C
ENST00000640146.2:c.718T>C ENSP00000491984.2:p.Phe240Leu
ENST00000650745.1:n.1203T>C
ENST00000650861.1:n.1974T>C
ENST00000650986.1:n.56T>C
ENST00000651459.1:c.164T>C
ENST00000651533.1:n.439T>C
ENST00000651668.1:n.330T>C
ENST00000651794.1:n.1236T>C
ENST00000651819.1:n.318T>C
ENST00000652579.1:n.653T>C
ENST00000652724.1:n.583T>C
ENST00000332351.7:c.1378T>C ENSP00000331327.3:p.Phe460Leu
ENST00000379077.7:c.*577T>C ENSP00000368368.3:n.*577T>C
ENST00000379079.6:c.742T>C ENSP00000368370.2:p.Phe248Leu
ENST00000448076.7:c.1378T>C ENSP00000413452.3:p.Phe460Leu
ENST00000452863.7:c.1327T>C ENSP00000415516.3:p.Phe443Leu
ENST00000527882.5:c.359T>C
ENST00000530998.5:c.691T>C ENSP00000435307.1:p.Phe231Leu
NM_000378.4:c.1327T>C NP_000369.3:p.Phe443Leu
NM_001198551.1:c.742T>C , LRG_525t2:c.742T>C NP_001185480.1:p.Phe248Leu
NM_001198552.1:c.691T>C NP_001185481.1:p.Phe231Leu
NM_024424.3:c.1378T>C NP_077742.2:p.Phe460Leu
NM_024426.4:c.1378T>C NP_077744.3:p.Phe460Leu
NM_000378.5:c.1342T>C NP_000369.4:p.Phe448Leu
NM_024424.4:c.1393T>C NP_077742.3:p.Phe465Leu
NM_024426.5:c.1393T>C NP_077744.4:p.Phe465Leu
NM_001367854.1:c.205T>C NP_001354783.1:p.Phe69Leu
NR_160306.1:n.1725T>C
NM_000378.6:c.1342T>C NP_000369.4:p.Phe448Leu
NM_001198552.2:c.691T>C NP_001185481.1:p.Phe231Leu
NM_024424.5:c.1393T>C NP_077742.3:p.Phe465Leu
NM_024426.6:c.1393T>C MANE Select NP_077744.4:p.Phe465Leu