Canonical Allele Identifier: CA645577477

Gene: WT1

Linked Data

• COSMIC: COSM28976

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392728_32392729insG , CM000673.2:g.32392728_32392729insG	GRCh38
NC_000011.9:g.32414274_32414275insG , CM000673.1:g.32414274_32414275insG	GRCh37
NC_000011.8:g.32370850_32370851insG	NCBI36
NG_009272.1:g.47813_47814insC , LRG_525:g.47813_47814insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1240_1241insC	ENSP00000331327.5:p.Lys414ThrfsTer4
ENST00000379077.9:c.*475_*476insC	ENSP00000368368.5:n.*475_*476insC
ENST00000379079.8:c.640_641insC	ENSP00000368370.2:p.Lys214ThrfsTer4
ENST00000448076.9:c.1291_1292insC	ENSP00000413452.5:p.Lys431ThrfsTer4
ENST00000452863.10:c.1291_1292insC MANE Select	ENSP00000415516.5:p.Lys431ThrfsTer4
ENST00000526685.2:n.745_746insC
ENST00000639563.3:c.1240_1241insC	ENSP00000492269.3:p.Lys414ThrfsTer4
ENST00000639907.2:n.434_435insC
ENST00000640146.2:c.616_617insC	ENSP00000491984.2:p.Lys206ThrfsTer4
ENST00000650745.1:n.500_501insC
ENST00000650861.1:n.1872_1873insC
ENST00000651459.1:c.62_63insC
ENST00000651533.1:n.337_338insC
ENST00000651668.1:n.228_229insC
ENST00000651794.1:n.1134_1135insC
ENST00000651819.1:n.216_217insC
ENST00000652579.1:n.551_552insC
ENST00000652724.1:n.481_482insC
ENST00000332351.7:c.1276_1277insC	ENSP00000331327.3:p.Lys426ThrfsTer4
ENST00000379077.7:c.*475_*476insC	ENSP00000368368.3:n.*475_*476insC
ENST00000379079.6:c.640_641insC	ENSP00000368370.2:p.Lys214ThrfsTer4
ENST00000448076.7:c.1276_1277insC	ENSP00000413452.3:p.Lys426ThrfsTer4
ENST00000452863.7:c.1225_1226insC	ENSP00000415516.3:p.Lys409ThrfsTer4
ENST00000527882.5:c.321-665_321-664insC
ENST00000530998.5:c.589_590insC	ENSP00000435307.1:p.Lys197ThrfsTer4
NM_000378.4:c.1225_1226insC	NP_000369.3:p.Lys409ThrfsTer4
NM_001198551.1:c.640_641insC , LRG_525t2:c.640_641insC	NP_001185480.1:p.Lys214ThrfsTer4
NM_001198552.1:c.589_590insC	NP_001185481.1:p.Lys197ThrfsTer4
NM_024424.3:c.1276_1277insC	NP_077742.2:p.Lys426ThrfsTer4
NM_024426.4:c.1276_1277insC	NP_077744.3:p.Lys426ThrfsTer4
NM_000378.5:c.1240_1241insC	NP_000369.4:p.Lys414ThrfsTer4
NM_024424.4:c.1291_1292insC	NP_077742.3:p.Lys431ThrfsTer4
NM_024426.5:c.1291_1292insC	NP_077744.4:p.Lys431ThrfsTer4
NM_001367854.1:c.103_104insC	NP_001354783.1:p.Lys35ThrfsTer4
NR_160306.1:n.1623_1624insC
NM_000378.6:c.1240_1241insC	NP_000369.4:p.Lys414ThrfsTer4
NM_001198552.2:c.589_590insC	NP_001185481.1:p.Lys197ThrfsTer4
NM_024424.5:c.1291_1292insC	NP_077742.3:p.Lys431ThrfsTer4
NM_024426.6:c.1291_1292insC MANE Select	NP_077744.4:p.Lys431ThrfsTer4