Canonical Allele Identifier: CA645577470

Gene: WT1

Linked Data

• COSMIC: COSM5879206 ; COSM5879207 ; COSM5879208

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392704delinsGGAAAT , CM000673.2:g.32392704delinsGGAAAT	GRCh38
NC_000011.9:g.32414250delinsGGAAAT , CM000673.1:g.32414250delinsGGAAAT	GRCh37
NC_000011.8:g.32370826delinsGGAAAT	NCBI36
NG_009272.1:g.47838delinsATTTCC , LRG_525:g.47838delinsATTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1265delinsATTTCC	ENSP00000331327.5:p.Arg422HisfsTer17
ENST00000379077.9:c.*500delinsATTTCC	ENSP00000368368.5:n.*500delinsATTTCC
ENST00000379079.8:c.665delinsATTTCC	ENSP00000368370.2:p.Arg222HisfsTer17
ENST00000448076.9:c.1316delinsATTTCC	ENSP00000413452.5:p.Arg439HisfsTer17
ENST00000452863.10:c.1316delinsATTTCC MANE Select	ENSP00000415516.5:p.Arg439HisfsTer17
ENST00000526685.2:n.770delinsATTTCC
ENST00000639563.3:c.1265delinsATTTCC	ENSP00000492269.3:p.Arg422HisfsTer17
ENST00000639907.2:n.459delinsATTTCC
ENST00000640146.2:c.641delinsATTTCC	ENSP00000491984.2:p.Arg214HisfsTer17
ENST00000650745.1:n.525delinsATTTCC
ENST00000650861.1:n.1897delinsATTTCC
ENST00000651459.1:c.87delinsATTTCC
ENST00000651533.1:n.362delinsATTTCC
ENST00000651668.1:n.253delinsATTTCC
ENST00000651794.1:n.1159delinsATTTCC
ENST00000651819.1:n.241delinsATTTCC
ENST00000652579.1:n.576delinsATTTCC
ENST00000652724.1:n.506delinsATTTCC
ENST00000332351.7:c.1301delinsATTTCC	ENSP00000331327.3:p.Arg434HisfsTer17
ENST00000379077.7:c.*500delinsATTTCC	ENSP00000368368.3:n.*500delinsATTTCC
ENST00000379079.6:c.665delinsATTTCC	ENSP00000368370.2:p.Arg222HisfsTer17
ENST00000448076.7:c.1301delinsATTTCC	ENSP00000413452.3:p.Arg434HisfsTer17
ENST00000452863.7:c.1250delinsATTTCC	ENSP00000415516.3:p.Arg417HisfsTer17
ENST00000527882.5:c.321-640delinsATTTCC
ENST00000530998.5:c.614delinsATTTCC	ENSP00000435307.1:p.Arg205HisfsTer17
NM_000378.4:c.1250delinsATTTCC	NP_000369.3:p.Arg417HisfsTer17
NM_001198551.1:c.665delinsATTTCC , LRG_525t2:c.665delinsATTTCC	NP_001185480.1:p.Arg222HisfsTer17
NM_001198552.1:c.614delinsATTTCC	NP_001185481.1:p.Arg205HisfsTer17
NM_024424.3:c.1301delinsATTTCC	NP_077742.2:p.Arg434HisfsTer17
NM_024426.4:c.1301delinsATTTCC	NP_077744.3:p.Arg434HisfsTer17
NM_000378.5:c.1265delinsATTTCC	NP_000369.4:p.Arg422HisfsTer17
NM_024424.4:c.1316delinsATTTCC	NP_077742.3:p.Arg439HisfsTer17
NM_024426.5:c.1316delinsATTTCC	NP_077744.4:p.Arg439HisfsTer17
NM_001367854.1:c.128delinsATTTCC	NP_001354783.1:p.Arg43HisfsTer17
NR_160306.1:n.1648delinsATTTCC
NM_000378.6:c.1265delinsATTTCC	NP_000369.4:p.Arg422HisfsTer17
NM_001198552.2:c.614delinsATTTCC	NP_001185481.1:p.Arg205HisfsTer17
NM_024424.5:c.1316delinsATTTCC	NP_077742.3:p.Arg439HisfsTer17
NM_024426.6:c.1316delinsATTTCC MANE Select	NP_077744.4:p.Arg439HisfsTer17