Canonical Allele Identifier: CA645577449

Gene: WT1

Linked Data

• COSMIC: COSM5945184

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392019_32392020delinsAC , CM000673.2:g.32392019_32392020delinsAC	GRCh38
NC_000011.9:g.32413565_32413566delinsAC , CM000673.1:g.32413565_32413566delinsAC	GRCh37
NC_000011.8:g.32370141_32370142delinsAC	NCBI36
NG_009272.1:g.48522_48523delinsGT , LRG_525:g.48522_48523delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1348_1349delinsGT	ENSP00000331327.5:p.Arg450Val
ENST00000379077.9:c.*583_*584delinsGT	ENSP00000368368.5:n.*583_*584delinsGT
ENST00000379079.8:c.748_749delinsGT	ENSP00000368370.2:p.Arg250Val
ENST00000448076.9:c.1399_1400delinsGT	ENSP00000413452.5:p.Arg467Val
ENST00000452863.10:c.1399_1400delinsGT MANE Select	ENSP00000415516.5:p.Arg467Val
ENST00000526685.2:n.853_854delinsGT
ENST00000639563.3:c.1348_1349delinsGT	ENSP00000492269.3:p.Arg450Val
ENST00000639907.2:n.542_543delinsGT
ENST00000640146.2:c.724_725delinsGT	ENSP00000491984.2:p.Arg242Val
ENST00000650745.1:n.1209_1210delinsGT
ENST00000650861.1:n.1980_1981delinsGT
ENST00000650986.1:n.62_63delinsGT
ENST00000651459.1:c.170_171delinsGT
ENST00000651533.1:n.445_446delinsGT
ENST00000651668.1:n.336_337delinsGT
ENST00000651794.1:n.1242_1243delinsGT
ENST00000651819.1:n.324_325delinsGT
ENST00000652579.1:n.659_660delinsGT
ENST00000652724.1:n.589_590delinsGT
ENST00000332351.7:c.1384_1385delinsGT	ENSP00000331327.3:p.Arg462Val
ENST00000379077.7:c.*583_*584delinsGT	ENSP00000368368.3:n.*583_*584delinsGT
ENST00000379079.6:c.748_749delinsGT	ENSP00000368370.2:p.Arg250Val
ENST00000448076.7:c.1384_1385delinsGT	ENSP00000413452.3:p.Arg462Val
ENST00000452863.7:c.1333_1334delinsGT	ENSP00000415516.3:p.Arg445Val
ENST00000527882.5:c.365_366delinsGT
ENST00000530998.5:c.697_698delinsGT	ENSP00000435307.1:p.Arg233Val
NM_000378.4:c.1333_1334delinsGT	NP_000369.3:p.Arg445Val
NM_001198551.1:c.748_749delinsGT , LRG_525t2:c.748_749delinsGT	NP_001185480.1:p.Arg250Val
NM_001198552.1:c.697_698delinsGT	NP_001185481.1:p.Arg233Val
NM_024424.3:c.1384_1385delinsGT	NP_077742.2:p.Arg462Val
NM_024426.4:c.1384_1385delinsGT	NP_077744.3:p.Arg462Val
NM_000378.5:c.1348_1349delinsGT	NP_000369.4:p.Arg450Val
NM_024424.4:c.1399_1400delinsGT	NP_077742.3:p.Arg467Val
NM_024426.5:c.1399_1400delinsGT	NP_077744.4:p.Arg467Val
NM_001367854.1:c.211_212delinsGT	NP_001354783.1:p.Arg71Val
NR_160306.1:n.1731_1732delinsGT
NM_000378.6:c.1348_1349delinsGT	NP_000369.4:p.Arg450Val
NM_001198552.2:c.697_698delinsGT	NP_001185481.1:p.Arg233Val
NM_024424.5:c.1399_1400delinsGT	NP_077742.3:p.Arg467Val
NM_024426.6:c.1399_1400delinsGT MANE Select	NP_077744.4:p.Arg467Val