Canonical Allele Identifier: CA2695213662

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392674_32392679del , CM000673.2:g.32392674_32392679del	GRCh38
NC_000011.9:g.32414220_32414225del , CM000673.1:g.32414220_32414225del	GRCh37
NC_000011.8:g.32370796_32370801del	NCBI36
NG_009272.1:g.47864_47869del , LRG_525:g.47864_47869del

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1291_1296del	ENSP00000331327.5:p.Arg431_Arg432del
ENST00000379077.9:c.*526_*531del	ENSP00000368368.5:n.*526_*531del
ENST00000379079.8:c.691_696del	ENSP00000368370.2:p.Arg231_Arg232del
ENST00000448076.9:c.1342_1347del	ENSP00000413452.5:p.Arg448_Arg449del
ENST00000452863.10:c.1342_1347del MANE Select	ENSP00000415516.5:p.Arg448_Arg449del
ENST00000526685.2:n.796_801del
ENST00000639563.3:c.1291_1296del	ENSP00000492269.3:p.Arg431_Arg432del
ENST00000639907.2:n.485_490del
ENST00000640146.2:c.667_672del	ENSP00000491984.2:p.Arg223_Arg224del
ENST00000650745.1:n.551_556del
ENST00000650861.1:n.1923_1928del
ENST00000651459.1:c.113_118del
ENST00000651533.1:n.388_393del
ENST00000651668.1:n.279_284del
ENST00000651794.1:n.1185_1190del
ENST00000651819.1:n.267_272del
ENST00000652579.1:n.602_607del
ENST00000652724.1:n.532_537del
ENST00000332351.7:c.1327_1332del	ENSP00000331327.3:p.Arg443_Arg444del
ENST00000379077.7:c.*526_*531del	ENSP00000368368.3:n.*526_*531del
ENST00000379079.6:c.691_696del	ENSP00000368370.2:p.Arg231_Arg232del
ENST00000448076.7:c.1327_1332del	ENSP00000413452.3:p.Arg443_Arg444del
ENST00000452863.7:c.1276_1281del	ENSP00000415516.3:p.Arg426_Arg427del
ENST00000527882.5:c.321-614_321-609del
ENST00000530998.5:c.640_645del	ENSP00000435307.1:p.Arg214_Arg215del
NM_000378.4:c.1276_1281del	NP_000369.3:p.Arg426_Arg427del
NM_001198551.1:c.691_696del , LRG_525t2:c.691_696del	NP_001185480.1:p.Arg231_Arg232del
NM_001198552.1:c.640_645del	NP_001185481.1:p.Arg214_Arg215del
NM_024424.3:c.1327_1332del	NP_077742.2:p.Arg443_Arg444del
NM_024426.4:c.1327_1332del	NP_077744.3:p.Arg443_Arg444del
NM_000378.5:c.1291_1296del	NP_000369.4:p.Arg431_Arg432del
NM_024424.4:c.1342_1347del	NP_077742.3:p.Arg448_Arg449del
NM_024426.5:c.1342_1347del	NP_077744.4:p.Arg448_Arg449del
NM_001367854.1:c.154_159del	NP_001354783.1:p.Arg52_Arg53del
NR_160306.1:n.1674_1679del
NM_000378.6:c.1291_1296del	NP_000369.4:p.Arg431_Arg432del
NM_001198552.2:c.640_645del	NP_001185481.1:p.Arg214_Arg215del
NM_024424.5:c.1342_1347del	NP_077742.3:p.Arg448_Arg449del
NM_024426.6:c.1342_1347del MANE Select	NP_077744.4:p.Arg448_Arg449del