Canonical Allele Identifier: CA891842091

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392029_32392030insGGGGCAAACTT , CM000673.2:g.32392029_32392030insGGGGCAAACTT	GRCh38
NC_000011.9:g.32413575_32413576insGGGGCAAACTT , CM000673.1:g.32413575_32413576insGGGGCAAACTT	GRCh37
NC_000011.8:g.32370151_32370152insGGGGCAAACTT	NCBI36
NG_009272.1:g.48517_48518insTGCCCCAAGTT , LRG_525:g.48517_48518insTGCCCCAAGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1343_1344insTGCCCCAAGTT	ENSP00000331327.5:p.Ser449AlafsTer10
ENST00000379077.9:c.*578_*579insTGCCCCAAGTT	ENSP00000368368.5:n.*578_*579insTGCCCCAAGTT
ENST00000379079.8:c.743_744insTGCCCCAAGTT	ENSP00000368370.2:p.Ser249AlafsTer10
ENST00000448076.9:c.1394_1395insTGCCCCAAGTT	ENSP00000413452.5:p.Ser466AlafsTer10
ENST00000452863.10:c.1394_1395insTGCCCCAAGTT MANE Select	ENSP00000415516.5:p.Ser466AlafsTer10
ENST00000526685.2:n.848_849insTGCCCCAAGTT
ENST00000639563.3:c.1343_1344insTGCCCCAAGTT	ENSP00000492269.3:p.Ser449AlafsTer10
ENST00000639907.2:n.537_538insTGCCCCAAGTT
ENST00000640146.2:c.719_720insTGCCCCAAGTT	ENSP00000491984.2:p.Ser241AlafsTer10
ENST00000650745.1:n.1204_1205insTGCCCCAAGTT
ENST00000650861.1:n.1975_1976insTGCCCCAAGTT
ENST00000650986.1:n.57_58insTGCCCCAAGTT
ENST00000651459.1:c.165_166insTGCCCCAAGTT
ENST00000651533.1:n.440_441insTGCCCCAAGTT
ENST00000651668.1:n.331_332insTGCCCCAAGTT
ENST00000651794.1:n.1237_1238insTGCCCCAAGTT
ENST00000651819.1:n.319_320insTGCCCCAAGTT
ENST00000652579.1:n.654_655insTGCCCCAAGTT
ENST00000652724.1:n.584_585insTGCCCCAAGTT
ENST00000332351.7:c.1379_1380insTGCCCCAAGTT	ENSP00000331327.3:p.Ser461AlafsTer10
ENST00000379077.7:c.*578_*579insTGCCCCAAGTT	ENSP00000368368.3:n.*578_*579insTGCCCCAAGTT
ENST00000379079.6:c.743_744insTGCCCCAAGTT	ENSP00000368370.2:p.Ser249AlafsTer10
ENST00000448076.7:c.1379_1380insTGCCCCAAGTT	ENSP00000413452.3:p.Ser461AlafsTer10
ENST00000452863.7:c.1328_1329insTGCCCCAAGTT	ENSP00000415516.3:p.Ser444AlafsTer10
ENST00000527882.5:c.360_361insTGCCCCAAGTT
ENST00000530998.5:c.692_693insTGCCCCAAGTT	ENSP00000435307.1:p.Ser232AlafsTer10
NM_000378.4:c.1328_1329insTGCCCCAAGTT	NP_000369.3:p.Ser444AlafsTer10
NM_001198551.1:c.743_744insTGCCCCAAGTT , LRG_525t2:c.743_744insTGCCCCAAGTT	NP_001185480.1:p.Ser249AlafsTer10
NM_001198552.1:c.692_693insTGCCCCAAGTT	NP_001185481.1:p.Ser232AlafsTer10
NM_024424.3:c.1379_1380insTGCCCCAAGTT	NP_077742.2:p.Ser461AlafsTer10
NM_024426.4:c.1379_1380insTGCCCCAAGTT	NP_077744.3:p.Ser461AlafsTer10
NM_000378.5:c.1343_1344insTGCCCCAAGTT	NP_000369.4:p.Ser449AlafsTer10
NM_024424.4:c.1394_1395insTGCCCCAAGTT	NP_077742.3:p.Ser466AlafsTer10
NM_024426.5:c.1394_1395insTGCCCCAAGTT	NP_077744.4:p.Ser466AlafsTer10
NM_001367854.1:c.206_207insTGCCCCAAGTT	NP_001354783.1:p.Ser70AlafsTer10
NR_160306.1:n.1726_1727insTGCCCCAAGTT
NM_000378.6:c.1343_1344insTGCCCCAAGTT	NP_000369.4:p.Ser449AlafsTer10
NM_001198552.2:c.692_693insTGCCCCAAGTT	NP_001185481.1:p.Ser232AlafsTer10
NM_024424.5:c.1394_1395insTGCCCCAAGTT	NP_077742.3:p.Ser466AlafsTer10
NM_024426.6:c.1394_1395insTGCCCCAAGTT MANE Select	NP_077744.4:p.Ser466AlafsTer10