Canonical Allele Identifier: CA645577462

Gene: WT1

Linked Data

• COSMIC: COSM5879200 ; COSM5879201 ; COSM5879202

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392672_32392675dup , CM000673.2:g.32392672_32392675dup	GRCh38
NC_000011.9:g.32414218_32414221dup , CM000673.1:g.32414218_32414221dup	GRCh37
NC_000011.8:g.32370794_32370797dup	NCBI36
NG_009272.1:g.47868_47871dup , LRG_525:g.47868_47871dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1295_1298dup	ENSP00000331327.5:p.His433GlnfsTer11
ENST00000379077.9:c.*530_*533dup	ENSP00000368368.5:n.*530_*533dup
ENST00000379079.8:c.695_698dup	ENSP00000368370.2:p.His233GlnfsTer11
ENST00000448076.9:c.1346_1349dup	ENSP00000413452.5:p.His450GlnfsTer11
ENST00000452863.10:c.1346_1349dup MANE Select	ENSP00000415516.5:p.His450GlnfsTer11
ENST00000526685.2:n.800_803dup
ENST00000639563.3:c.1295_1298dup	ENSP00000492269.3:p.His433GlnfsTer11
ENST00000639907.2:n.489_492dup
ENST00000640146.2:c.671_674dup	ENSP00000491984.2:p.His225GlnfsTer11
ENST00000650745.1:n.555_558dup
ENST00000650861.1:n.1927_1930dup
ENST00000651459.1:c.117_120dup
ENST00000651533.1:n.392_395dup
ENST00000651668.1:n.283_286dup
ENST00000651794.1:n.1189_1192dup
ENST00000651819.1:n.271_274dup
ENST00000652579.1:n.606_609dup
ENST00000652724.1:n.536_539dup
ENST00000332351.7:c.1331_1334dup	ENSP00000331327.3:p.His445GlnfsTer11
ENST00000379077.7:c.*530_*533dup	ENSP00000368368.3:n.*530_*533dup
ENST00000379079.6:c.695_698dup	ENSP00000368370.2:p.His233GlnfsTer11
ENST00000448076.7:c.1331_1334dup	ENSP00000413452.3:p.His445GlnfsTer11
ENST00000452863.7:c.1280_1283dup	ENSP00000415516.3:p.His428GlnfsTer11
ENST00000527882.5:c.321-610_321-607dup
ENST00000530998.5:c.644_647dup	ENSP00000435307.1:p.His216GlnfsTer11
NM_000378.4:c.1280_1283dup	NP_000369.3:p.His428GlnfsTer11
NM_001198551.1:c.695_698dup , LRG_525t2:c.695_698dup	NP_001185480.1:p.His233GlnfsTer11
NM_001198552.1:c.644_647dup	NP_001185481.1:p.His216GlnfsTer11
NM_024424.3:c.1331_1334dup	NP_077742.2:p.His445GlnfsTer11
NM_024426.4:c.1331_1334dup	NP_077744.3:p.His445GlnfsTer11
NM_000378.5:c.1295_1298dup	NP_000369.4:p.His433GlnfsTer11
NM_024424.4:c.1346_1349dup	NP_077742.3:p.His450GlnfsTer11
NM_024426.5:c.1346_1349dup	NP_077744.4:p.His450GlnfsTer11
NM_001367854.1:c.158_161dup	NP_001354783.1:p.His54GlnfsTer11
NR_160306.1:n.1678_1681dup
NM_000378.6:c.1295_1298dup	NP_000369.4:p.His433GlnfsTer11
NM_001198552.2:c.644_647dup	NP_001185481.1:p.His216GlnfsTer11
NM_024424.5:c.1346_1349dup	NP_077742.3:p.His450GlnfsTer11
NM_024426.6:c.1346_1349dup MANE Select	NP_077744.4:p.His450GlnfsTer11