Canonical Allele Identifier: CA2790961091

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392032_32392033del , CM000673.2:g.32392032_32392033del	GRCh38
NC_000011.9:g.32413578_32413579del , CM000673.1:g.32413578_32413579del	GRCh37
NC_000011.8:g.32370154_32370155del	NCBI36
NG_009272.1:g.48510_48511del , LRG_525:g.48510_48511del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1336_1337del	ENSP00000331327.5:p.Arg446LysfsTer18
ENST00000379077.9:c.*571_*572del	ENSP00000368368.5:n.*571_*572del
ENST00000379079.8:c.736_737del	ENSP00000368370.2:p.Arg246LysfsTer18
ENST00000448076.9:c.1387_1388del	ENSP00000413452.5:p.Arg463LysfsTer18
ENST00000452863.10:c.1387_1388del MANE Select	ENSP00000415516.5:p.Arg463LysfsTer18
ENST00000526685.2:n.841_842del
ENST00000639563.3:c.1336_1337del	ENSP00000492269.3:p.Arg446LysfsTer18
ENST00000639907.2:n.530_531del
ENST00000640146.2:c.712_713del	ENSP00000491984.2:p.Arg238LysfsTer18
ENST00000650745.1:n.1197_1198del
ENST00000650861.1:n.1968_1969del
ENST00000650986.1:n.50_51del
ENST00000651459.1:c.158_159del
ENST00000651533.1:n.433_434del
ENST00000651668.1:n.324_325del
ENST00000651794.1:n.1230_1231del
ENST00000651819.1:n.312_313del
ENST00000652579.1:n.647_648del
ENST00000652724.1:n.577_578del
ENST00000332351.7:c.1372_1373del	ENSP00000331327.3:p.Arg458LysfsTer18
ENST00000379077.7:c.*571_*572del	ENSP00000368368.3:n.*571_*572del
ENST00000379079.6:c.736_737del	ENSP00000368370.2:p.Arg246LysfsTer18
ENST00000448076.7:c.1372_1373del	ENSP00000413452.3:p.Arg458LysfsTer18
ENST00000452863.7:c.1321_1322del	ENSP00000415516.3:p.Arg441LysfsTer18
ENST00000527882.5:c.353_354del
ENST00000530998.5:c.685_686del	ENSP00000435307.1:p.Arg229LysfsTer18
NM_000378.4:c.1321_1322del	NP_000369.3:p.Arg441LysfsTer18
NM_001198551.1:c.736_737del , LRG_525t2:c.736_737del	NP_001185480.1:p.Arg246LysfsTer18
NM_001198552.1:c.685_686del	NP_001185481.1:p.Arg229LysfsTer18
NM_024424.3:c.1372_1373del	NP_077742.2:p.Arg458LysfsTer18
NM_024426.4:c.1372_1373del	NP_077744.3:p.Arg458LysfsTer18
NM_000378.5:c.1336_1337del	NP_000369.4:p.Arg446LysfsTer18
NM_024424.4:c.1387_1388del	NP_077742.3:p.Arg463LysfsTer18
NM_024426.5:c.1387_1388del	NP_077744.4:p.Arg463LysfsTer18
NM_001367854.1:c.199_200del	NP_001354783.1:p.Arg67LysfsTer18
NR_160306.1:n.1719_1720del
NM_000378.6:c.1336_1337del	NP_000369.4:p.Arg446LysfsTer18
NM_001198552.2:c.685_686del	NP_001185481.1:p.Arg229LysfsTer18
NM_024424.5:c.1387_1388del	NP_077742.3:p.Arg463LysfsTer18
NM_024426.6:c.1387_1388del MANE Select	NP_077744.4:p.Arg463LysfsTer18