Canonical Allele Identifier: CA645577697

Gene: WT1

Linked Data

• COSMIC: COSM5879323 ; COSM5879324 ; COSM5879325

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399975_32399981del , CM000673.2:g.32399975_32399981del	GRCh38
NC_000011.9:g.32421521_32421527del , CM000673.1:g.32421521_32421527del	GRCh37
NC_000011.8:g.32378097_32378103del	NCBI36
NG_009272.1:g.40562_40568del , LRG_525:g.40562_40568del

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1030_1036del	ENSP00000331327.5:p.Ile344ArgfsTer17
ENST00000379077.9:c.*265_*271del	ENSP00000368368.5:n.*265_*271del
ENST00000379079.8:c.430_436del	ENSP00000368370.2:p.Ile144ArgfsTer17
ENST00000448076.9:c.1081_1087del	ENSP00000413452.5:p.Ile361ArgfsTer17
ENST00000452863.10:c.1081_1087del MANE Select	ENSP00000415516.5:p.Ile361ArgfsTer17
ENST00000526685.2:n.535_541del
ENST00000639563.3:c.1030_1036del	ENSP00000492269.3:p.Ile344ArgfsTer17
ENST00000639907.2:n.224_230del
ENST00000640146.2:c.406_412del	ENSP00000491984.2:p.Ile136ArgfsTer17
ENST00000651459.1:c.3_9del
ENST00000651794.1:n.824_830del
ENST00000652579.1:n.241_247del
ENST00000652724.1:n.271_277del
ENST00000332351.7:c.1066_1072del	ENSP00000331327.3:p.Ile356ArgfsTer17
ENST00000379077.7:c.*265_*271del	ENSP00000368368.3:n.*265_*271del
ENST00000379079.6:c.430_436del	ENSP00000368370.2:p.Ile144ArgfsTer17
ENST00000448076.7:c.1066_1072del	ENSP00000413452.3:p.Ile356ArgfsTer17
ENST00000452863.7:c.1015_1021del	ENSP00000415516.3:p.Ile339ArgfsTer17
ENST00000526685.1:c.-108_-102del	ENSP00000436292.1:n.-108_-102del
ENST00000527775.1:c.319_325del	ENSP00000435351.1:p.Ile107ArgfsTer17
ENST00000527882.5:c.137_143del
ENST00000530998.5:c.379_385del	ENSP00000435307.1:p.Ile127ArgfsTer17
NM_000378.4:c.1015_1021del	NP_000369.3:p.Ile339ArgfsTer17
NM_001198551.1:c.430_436del , LRG_525t2:c.430_436del	NP_001185480.1:p.Ile144ArgfsTer17
NM_001198552.1:c.379_385del	NP_001185481.1:p.Ile127ArgfsTer17
NM_024424.3:c.1066_1072del	NP_077742.2:p.Ile356ArgfsTer17
NM_024426.4:c.1066_1072del	NP_077744.3:p.Ile356ArgfsTer17
NM_000378.5:c.1030_1036del	NP_000369.4:p.Ile344ArgfsTer17
NM_024424.4:c.1081_1087del	NP_077742.3:p.Ile361ArgfsTer17
NM_024426.5:c.1081_1087del	NP_077744.4:p.Ile361ArgfsTer17
NM_001367854.1:c.-108_-102del	NP_001354783.1:n.-108_-102del
NR_160306.1:n.1413_1419del
NM_000378.6:c.1030_1036del	NP_000369.4:p.Ile344ArgfsTer17
NM_001198552.2:c.379_385del	NP_001185481.1:p.Ile127ArgfsTer17
NM_024424.5:c.1081_1087del	NP_077742.3:p.Ile361ArgfsTer17
NM_024426.6:c.1081_1087del MANE Select	NP_077744.4:p.Ile361ArgfsTer17