Canonical Allele Identifier: CA2695213659

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391992_32392003del , CM000673.2:g.32391992_32392003del	GRCh38
NC_000011.9:g.32413538_32413549del , CM000673.1:g.32413538_32413549del	GRCh37
NC_000011.8:g.32370114_32370125del	NCBI36
NG_009272.1:g.48542_48553del , LRG_525:g.48542_48553del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1368_1379del	ENSP00000331327.5:p.His457_Thr460del
ENST00000379077.9:c.*603_*614del	ENSP00000368368.5:n.*603_*614del
ENST00000379079.8:c.768_779del	ENSP00000368370.2:p.His257_Thr260del
ENST00000448076.9:c.1419_1430del	ENSP00000413452.5:p.His474_Thr477del
ENST00000452863.10:c.1419_1430del MANE Select	ENSP00000415516.5:p.His474_Thr477del
ENST00000526685.2:n.873_884del
ENST00000639563.3:c.1368_1379del	ENSP00000492269.3:p.His457_Thr460del
ENST00000639907.2:n.562_573del
ENST00000640146.2:c.744_755del	ENSP00000491984.2:p.His249_Thr252del
ENST00000650745.1:n.1229_1240del
ENST00000650861.1:n.2000_2011del
ENST00000650986.1:n.82_93del
ENST00000651459.1:c.190_201del
ENST00000651533.1:n.465_476del
ENST00000651668.1:n.356_367del
ENST00000651794.1:n.1262_1273del
ENST00000651819.1:n.344_355del
ENST00000652579.1:n.679_690del
ENST00000652724.1:n.609_620del
ENST00000332351.7:c.1404_1415del	ENSP00000331327.3:p.His469_Thr472del
ENST00000379077.7:c.*603_*614del	ENSP00000368368.3:n.*603_*614del
ENST00000379079.6:c.768_779del	ENSP00000368370.2:p.His257_Thr260del
ENST00000448076.7:c.1404_1415del	ENSP00000413452.3:p.His469_Thr472del
ENST00000452863.7:c.1353_1364del	ENSP00000415516.3:p.His452_Thr455del
ENST00000527882.5:c.385_396del
ENST00000530998.5:c.717_728del	ENSP00000435307.1:p.His240_Thr243del
NM_000378.4:c.1353_1364del	NP_000369.3:p.His452_Thr455del
NM_001198551.1:c.768_779del , LRG_525t2:c.768_779del	NP_001185480.1:p.His257_Thr260del
NM_001198552.1:c.717_728del	NP_001185481.1:p.His240_Thr243del
NM_024424.3:c.1404_1415del	NP_077742.2:p.His469_Thr472del
NM_024426.4:c.1404_1415del	NP_077744.3:p.His469_Thr472del
NM_000378.5:c.1368_1379del	NP_000369.4:p.His457_Thr460del
NM_024424.4:c.1419_1430del	NP_077742.3:p.His474_Thr477del
NM_024426.5:c.1419_1430del	NP_077744.4:p.His474_Thr477del
NM_001367854.1:c.231_242del	NP_001354783.1:p.His78_Thr81del
NR_160306.1:n.1751_1762del
NM_000378.6:c.1368_1379del	NP_000369.4:p.His457_Thr460del
NM_001198552.2:c.717_728del	NP_001185481.1:p.His240_Thr243del
NM_024424.5:c.1419_1430del	NP_077742.3:p.His474_Thr477del
NM_024426.6:c.1419_1430del MANE Select	NP_077744.4:p.His474_Thr477del