Canonical Allele Identifier: CA379959261
Gene: WT1 HGNC NCBI

Linked Data

dbSNP Id: rs2132920415

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392707G>A , CM000673.2:g.32392707G>A GRCh38
NC_000011.9:g.32414253G>A , CM000673.1:g.32414253G>A GRCh37
NC_000011.8:g.32370829G>A NCBI36
NG_009272.1:g.47835C>T , LRG_525:g.47835C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1262C>T ENSP00000331327.5:p.Ser421Phe
ENST00000379077.9:c.*497C>T ENSP00000368368.5:n.*497C>T
ENST00000379079.8:c.662C>T ENSP00000368370.2:p.Ser221Phe
ENST00000448076.9:c.1313C>T ENSP00000413452.5:p.Ser438Phe
ENST00000452863.10:c.1313C>T MANE Select ENSP00000415516.5:p.Ser438Phe
ENST00000526685.2:n.767C>T
ENST00000639563.3:c.1262C>T ENSP00000492269.3:p.Ser421Phe
ENST00000639907.2:n.456C>T
ENST00000640146.2:c.638C>T ENSP00000491984.2:p.Ser213Phe
ENST00000650745.1:n.522C>T
ENST00000650861.1:n.1894C>T
ENST00000651459.1:c.84C>T
ENST00000651533.1:n.359C>T
ENST00000651668.1:n.250C>T
ENST00000651794.1:n.1156C>T
ENST00000651819.1:n.238C>T
ENST00000652579.1:n.573C>T
ENST00000652724.1:n.503C>T
ENST00000332351.7:c.1298C>T ENSP00000331327.3:p.Ser433Phe
ENST00000379077.7:c.*497C>T ENSP00000368368.3:n.*497C>T
ENST00000379079.6:c.662C>T ENSP00000368370.2:p.Ser221Phe
ENST00000448076.7:c.1298C>T ENSP00000413452.3:p.Ser433Phe
ENST00000452863.7:c.1247C>T ENSP00000415516.3:p.Ser416Phe
ENST00000527882.5:c.321-643C>T
ENST00000530998.5:c.611C>T ENSP00000435307.1:p.Ser204Phe
NM_000378.4:c.1247C>T NP_000369.3:p.Ser416Phe
NM_001198551.1:c.662C>T , LRG_525t2:c.662C>T NP_001185480.1:p.Ser221Phe
NM_001198552.1:c.611C>T NP_001185481.1:p.Ser204Phe
NM_024424.3:c.1298C>T NP_077742.2:p.Ser433Phe
NM_024426.4:c.1298C>T NP_077744.3:p.Ser433Phe
NM_000378.5:c.1262C>T NP_000369.4:p.Ser421Phe
NM_024424.4:c.1313C>T NP_077742.3:p.Ser438Phe
NM_024426.5:c.1313C>T NP_077744.4:p.Ser438Phe
NM_001367854.1:c.125C>T NP_001354783.1:p.Ser42Phe
NR_160306.1:n.1645C>T
NM_000378.6:c.1262C>T NP_000369.4:p.Ser421Phe
NM_001198552.2:c.611C>T NP_001185481.1:p.Ser204Phe
NM_024424.5:c.1313C>T NP_077742.3:p.Ser438Phe
NM_024426.6:c.1313C>T MANE Select NP_077744.4:p.Ser438Phe