Canonical Allele Identifier: CA379959335
Gene: WT1 HGNC NCBI

Linked Data

dbSNP Id: rs2132920802

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392722C>A , CM000673.2:g.32392722C>A GRCh38
NC_000011.9:g.32414268C>A , CM000673.1:g.32414268C>A GRCh37
NC_000011.8:g.32370844C>A NCBI36
NG_009272.1:g.47820G>T , LRG_525:g.47820G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1247G>T ENSP00000331327.5:p.Cys416Phe
ENST00000379077.9:c.*482G>T ENSP00000368368.5:n.*482G>T
ENST00000379079.8:c.647G>T ENSP00000368370.2:p.Cys216Phe
ENST00000448076.9:c.1298G>T ENSP00000413452.5:p.Cys433Phe
ENST00000452863.10:c.1298G>T MANE Select ENSP00000415516.5:p.Cys433Phe
ENST00000526685.2:n.752G>T
ENST00000639563.3:c.1247G>T ENSP00000492269.3:p.Cys416Phe
ENST00000639907.2:n.441G>T
ENST00000640146.2:c.623G>T ENSP00000491984.2:p.Cys208Phe
ENST00000650745.1:n.507G>T
ENST00000650861.1:n.1879G>T
ENST00000651459.1:c.69G>T
ENST00000651533.1:n.344G>T
ENST00000651668.1:n.235G>T
ENST00000651794.1:n.1141G>T
ENST00000651819.1:n.223G>T
ENST00000652579.1:n.558G>T
ENST00000652724.1:n.488G>T
ENST00000332351.7:c.1283G>T ENSP00000331327.3:p.Cys428Phe
ENST00000379077.7:c.*482G>T ENSP00000368368.3:n.*482G>T
ENST00000379079.6:c.647G>T ENSP00000368370.2:p.Cys216Phe
ENST00000448076.7:c.1283G>T ENSP00000413452.3:p.Cys428Phe
ENST00000452863.7:c.1232G>T ENSP00000415516.3:p.Cys411Phe
ENST00000527882.5:c.321-658G>T
ENST00000530998.5:c.596G>T ENSP00000435307.1:p.Cys199Phe
NM_000378.4:c.1232G>T NP_000369.3:p.Cys411Phe
NM_001198551.1:c.647G>T , LRG_525t2:c.647G>T NP_001185480.1:p.Cys216Phe
NM_001198552.1:c.596G>T NP_001185481.1:p.Cys199Phe
NM_024424.3:c.1283G>T NP_077742.2:p.Cys428Phe
NM_024426.4:c.1283G>T NP_077744.3:p.Cys428Phe
NM_000378.5:c.1247G>T NP_000369.4:p.Cys416Phe
NM_024424.4:c.1298G>T NP_077742.3:p.Cys433Phe
NM_024426.5:c.1298G>T NP_077744.4:p.Cys433Phe
NM_001367854.1:c.110G>T NP_001354783.1:p.Cys37Phe
NR_160306.1:n.1630G>T
NM_000378.6:c.1247G>T NP_000369.4:p.Cys416Phe
NM_001198552.2:c.596G>T NP_001185481.1:p.Cys199Phe
NM_024424.5:c.1298G>T NP_077742.3:p.Cys433Phe
NM_024426.6:c.1298G>T MANE Select NP_077744.4:p.Cys433Phe