Canonical Allele Identifier: CA379958984
Gene: WT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392051G>T , CM000673.2:g.32392051G>T GRCh38
NC_000011.9:g.32413597G>T , CM000673.1:g.32413597G>T GRCh37
NC_000011.8:g.32370173G>T NCBI36
NG_009272.1:g.48491C>A , LRG_525:g.48491C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1317C>A ENSP00000331327.5:p.Phe439Leu
ENST00000379077.9:c.*552C>A ENSP00000368368.5:n.*552C>A
ENST00000379079.8:c.717C>A ENSP00000368370.2:p.Phe239Leu
ENST00000448076.9:c.1368C>A ENSP00000413452.5:p.Phe456Leu
ENST00000452863.10:c.1368C>A MANE Select ENSP00000415516.5:p.Phe456Leu
ENST00000526685.2:n.822C>A
ENST00000639563.3:c.1317C>A ENSP00000492269.3:p.Phe439Leu
ENST00000639907.2:n.511C>A
ENST00000640146.2:c.693C>A ENSP00000491984.2:p.Phe231Leu
ENST00000650745.1:n.1178C>A
ENST00000650861.1:n.1949C>A
ENST00000650986.1:n.31C>A
ENST00000651459.1:c.139C>A
ENST00000651533.1:n.414C>A
ENST00000651668.1:n.305C>A
ENST00000651794.1:n.1211C>A
ENST00000651819.1:n.293C>A
ENST00000652579.1:n.628C>A
ENST00000652724.1:n.558C>A
ENST00000332351.7:c.1353C>A ENSP00000331327.3:p.Phe451Leu
ENST00000379077.7:c.*552C>A ENSP00000368368.3:n.*552C>A
ENST00000379079.6:c.717C>A ENSP00000368370.2:p.Phe239Leu
ENST00000448076.7:c.1353C>A ENSP00000413452.3:p.Phe451Leu
ENST00000452863.7:c.1302C>A ENSP00000415516.3:p.Phe434Leu
ENST00000527882.5:c.334C>A
ENST00000530998.5:c.666C>A ENSP00000435307.1:p.Phe222Leu
NM_000378.4:c.1302C>A NP_000369.3:p.Phe434Leu
NM_001198551.1:c.717C>A , LRG_525t2:c.717C>A NP_001185480.1:p.Phe239Leu
NM_001198552.1:c.666C>A NP_001185481.1:p.Phe222Leu
NM_024424.3:c.1353C>A NP_077742.2:p.Phe451Leu
NM_024426.4:c.1353C>A NP_077744.3:p.Phe451Leu
NM_000378.5:c.1317C>A NP_000369.4:p.Phe439Leu
NM_024424.4:c.1368C>A NP_077742.3:p.Phe456Leu
NM_024426.5:c.1368C>A NP_077744.4:p.Phe456Leu
NM_001367854.1:c.180C>A NP_001354783.1:p.Phe60Leu
NR_160306.1:n.1700C>A
NM_000378.6:c.1317C>A NP_000369.4:p.Phe439Leu
NM_001198552.2:c.666C>A NP_001185481.1:p.Phe222Leu
NM_024424.5:c.1368C>A NP_077742.3:p.Phe456Leu
NM_024426.6:c.1368C>A MANE Select NP_077744.4:p.Phe456Leu