Canonical Allele Identifier: CA645577452

Gene: WT1

Linked Data

• COSMIC: COSM28975

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392026_32392027insT , CM000673.2:g.32392026_32392027insT	GRCh38
NC_000011.9:g.32413572_32413573insT , CM000673.1:g.32413572_32413573insT	GRCh37
NC_000011.8:g.32370148_32370149insT	NCBI36
NG_009272.1:g.48515_48516insA , LRG_525:g.48515_48516insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1341_1342insA	ENSP00000331327.5:p.Phe448IlefsTer17
ENST00000379077.9:c.*576_*577insA	ENSP00000368368.5:n.*576_*577insA
ENST00000379079.8:c.741_742insA	ENSP00000368370.2:p.Phe248IlefsTer17
ENST00000448076.9:c.1392_1393insA	ENSP00000413452.5:p.Phe465IlefsTer17
ENST00000452863.10:c.1392_1393insA MANE Select	ENSP00000415516.5:p.Phe465IlefsTer17
ENST00000526685.2:n.846_847insA
ENST00000639563.3:c.1341_1342insA	ENSP00000492269.3:p.Phe448IlefsTer17
ENST00000639907.2:n.535_536insA
ENST00000640146.2:c.717_718insA	ENSP00000491984.2:p.Phe240IlefsTer17
ENST00000650745.1:n.1202_1203insA
ENST00000650861.1:n.1973_1974insA
ENST00000650986.1:n.55_56insA
ENST00000651459.1:c.163_164insA
ENST00000651533.1:n.438_439insA
ENST00000651668.1:n.329_330insA
ENST00000651794.1:n.1235_1236insA
ENST00000651819.1:n.317_318insA
ENST00000652579.1:n.652_653insA
ENST00000652724.1:n.582_583insA
ENST00000332351.7:c.1377_1378insA	ENSP00000331327.3:p.Phe460IlefsTer17
ENST00000379077.7:c.*576_*577insA	ENSP00000368368.3:n.*576_*577insA
ENST00000379079.6:c.741_742insA	ENSP00000368370.2:p.Phe248IlefsTer17
ENST00000448076.7:c.1377_1378insA	ENSP00000413452.3:p.Phe460IlefsTer17
ENST00000452863.7:c.1326_1327insA	ENSP00000415516.3:p.Phe443IlefsTer17
ENST00000527882.5:c.358_359insA
ENST00000530998.5:c.690_691insA	ENSP00000435307.1:p.Phe231IlefsTer17
NM_000378.4:c.1326_1327insA	NP_000369.3:p.Phe443IlefsTer17
NM_001198551.1:c.741_742insA , LRG_525t2:c.741_742insA	NP_001185480.1:p.Phe248IlefsTer17
NM_001198552.1:c.690_691insA	NP_001185481.1:p.Phe231IlefsTer17
NM_024424.3:c.1377_1378insA	NP_077742.2:p.Phe460IlefsTer17
NM_024426.4:c.1377_1378insA	NP_077744.3:p.Phe460IlefsTer17
NM_000378.5:c.1341_1342insA	NP_000369.4:p.Phe448IlefsTer17
NM_024424.4:c.1392_1393insA	NP_077742.3:p.Phe465IlefsTer17
NM_024426.5:c.1392_1393insA	NP_077744.4:p.Phe465IlefsTer17
NM_001367854.1:c.204_205insA	NP_001354783.1:p.Phe69IlefsTer17
NR_160306.1:n.1724_1725insA
NM_000378.6:c.1341_1342insA	NP_000369.4:p.Phe448IlefsTer17
NM_001198552.2:c.690_691insA	NP_001185481.1:p.Phe231IlefsTer17
NM_024424.5:c.1392_1393insA	NP_077742.3:p.Phe465IlefsTer17
NM_024426.6:c.1392_1393insA MANE Select	NP_077744.4:p.Phe465IlefsTer17