Canonical Allele Identifier: CA1962335234

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391936_32391937delinsAT , CM000673.2:g.32391936_32391937delinsAT	GRCh38
NC_000011.9:g.32413482_32413483delinsAT , CM000673.1:g.32413482_32413483delinsAT	GRCh37
NC_000011.8:g.32370058_32370059delinsAT	NCBI36
NG_009272.1:g.48605_48606delinsAT , LRG_525:g.48605_48606delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1387+44_1387+45delinsAT	ENSP00000331327.5:n.1387+44_1387+45delinsAT
ENST00000379077.9:c.*631+35_*631+36delinsAT	ENSP00000368368.5:n.*631+35_*631+36delinsAT
ENST00000379079.8:c.787+44_787+45delinsAT	ENSP00000368370.2:n.787+44_787+45delinsAT
ENST00000448076.9:c.1438+44_1438+45delinsAT	ENSP00000413452.5:n.1438+44_1438+45delinsAT
ENST00000452863.10:c.1447+35_1447+36delinsAT MANE Select	ENSP00000415516.5:n.1447+35_1447+36delinsAT
ENST00000526685.2:n.892+44_892+45delinsAT
ENST00000639563.3:c.1396+35_1396+36delinsAT	ENSP00000492269.3:n.1396+35_1396+36delinsAT
ENST00000639907.2:n.581+44_581+45delinsAT
ENST00000640146.2:c.772+35_772+36delinsAT	ENSP00000491984.2:n.772+35_772+36delinsAT
ENST00000650745.1:n.1257+35_1257+36delinsAT
ENST00000650861.1:n.2019+44_2019+45delinsAT
ENST00000650986.1:n.110+35_110+36delinsAT
ENST00000651459.1:c.218+35_218+36delinsAT
ENST00000651533.1:n.484+44_484+45delinsAT
ENST00000651668.1:n.384+35_384+36delinsAT
ENST00000651794.1:n.1290+35_1290+36delinsAT
ENST00000651819.1:n.372+35_372+36delinsAT
ENST00000652579.1:n.707+35_707+36delinsAT
ENST00000652724.1:n.637+35_637+36delinsAT
ENST00000332351.7:c.1432+35_1432+36delinsAT	ENSP00000331327.3:n.1432+35_1432+36delinsAT
ENST00000379077.7:c.*631+35_*631+36delinsAT	ENSP00000368368.3:n.*631+35_*631+36delinsAT
ENST00000379079.6:c.787+44_787+45delinsAT	ENSP00000368370.2:n.787+44_787+45delinsAT
ENST00000448076.7:c.1423+44_1423+45delinsAT	ENSP00000413452.3:n.1423+44_1423+45delinsAT
ENST00000452863.7:c.1372+44_1372+45delinsAT	ENSP00000415516.3:n.1372+44_1372+45delinsAT
ENST00000527882.5:c.413+35_413+36delinsAT
ENST00000530998.5:c.745+35_745+36delinsAT	ENSP00000435307.1:n.745+35_745+36delinsAT
NM_000378.4:c.1372+44_1372+45delinsAT	NP_000369.3:n.1372+44_1372+45delinsAT
NM_001198551.1:c.787+44_787+45delinsAT , LRG_525t2:c.787+44_787+45delinsAT	NP_001185480.1:n.787+44_787+45delinsAT
NM_001198552.1:c.745+35_745+36delinsAT	NP_001185481.1:n.745+35_745+36delinsAT
NM_024424.3:c.1423+44_1423+45delinsAT	NP_077742.2:n.1423+44_1423+45delinsAT
NM_024426.4:c.1432+35_1432+36delinsAT	NP_077744.3:n.1432+35_1432+36delinsAT
NM_000378.5:c.1387+44_1387+45delinsAT	NP_000369.4:n.1387+44_1387+45delinsAT
NM_024424.4:c.1438+44_1438+45delinsAT	NP_077742.3:n.1438+44_1438+45delinsAT
NM_024426.5:c.1447+35_1447+36delinsAT	NP_077744.4:n.1447+35_1447+36delinsAT
NM_001367854.1:c.259+35_259+36delinsAT	NP_001354783.1:n.259+35_259+36delinsAT
NR_160306.1:n.1779+35_1779+36delinsAT
NM_000378.6:c.1387+44_1387+45delinsAT	NP_000369.4:n.1387+44_1387+45delinsAT
NM_001198552.2:c.745+35_745+36delinsAT	NP_001185481.1:n.745+35_745+36delinsAT
NM_024424.5:c.1438+44_1438+45delinsAT	NP_077742.3:n.1438+44_1438+45delinsAT
NM_024426.6:c.1447+35_1447+36delinsAT MANE Select	NP_077744.4:n.1447+35_1447+36delinsAT