Canonical Allele Identifier: CA1962335504

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392578_32392579delinsCA , CM000673.2:g.32392578_32392579delinsCA	GRCh38
NC_000011.9:g.32414124_32414125delinsCA , CM000673.1:g.32414124_32414125delinsCA	GRCh37
NC_000011.8:g.32370700_32370701delinsCA	NCBI36
NG_009272.1:g.47963_47964delinsTG , LRG_525:g.47963_47964delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1303+87_1303+88delinsTG	ENSP00000331327.5:n.1303+87_1303+88delinsTG
ENST00000379077.9:c.*538+87_*538+88delinsTG	ENSP00000368368.5:n.*538+87_*538+88delinsTG
ENST00000379079.8:c.703+87_703+88delinsTG	ENSP00000368370.2:n.703+87_703+88delinsTG
ENST00000448076.9:c.1354+87_1354+88delinsTG	ENSP00000413452.5:n.1354+87_1354+88delinsTG
ENST00000452863.10:c.1354+87_1354+88delinsTG MANE Select	ENSP00000415516.5:n.1354+87_1354+88delinsTG
ENST00000526685.2:n.808+87_808+88delinsTG
ENST00000639563.3:c.1303+87_1303+88delinsTG	ENSP00000492269.3:n.1303+87_1303+88delinsTG
ENST00000639907.2:n.497+87_497+88delinsTG
ENST00000640146.2:c.679+87_679+88delinsTG	ENSP00000491984.2:n.679+87_679+88delinsTG
ENST00000650745.1:n.650_651delinsTG
ENST00000650861.1:n.1935+87_1935+88delinsTG
ENST00000651459.1:c.125+87_125+88delinsTG
ENST00000651533.1:n.400+87_400+88delinsTG
ENST00000651668.1:n.291+87_291+88delinsTG
ENST00000651794.1:n.1197+87_1197+88delinsTG
ENST00000651819.1:n.279+87_279+88delinsTG
ENST00000652579.1:n.614+87_614+88delinsTG
ENST00000652724.1:n.544+87_544+88delinsTG
ENST00000332351.7:c.1339+87_1339+88delinsTG	ENSP00000331327.3:n.1339+87_1339+88delinsTG
ENST00000379077.7:c.*538+87_*538+88delinsTG	ENSP00000368368.3:n.*538+87_*538+88delinsTG
ENST00000379079.6:c.703+87_703+88delinsTG	ENSP00000368370.2:n.703+87_703+88delinsTG
ENST00000448076.7:c.1339+87_1339+88delinsTG	ENSP00000413452.3:n.1339+87_1339+88delinsTG
ENST00000452863.7:c.1288+87_1288+88delinsTG	ENSP00000415516.3:n.1288+87_1288+88delinsTG
ENST00000527882.5:c.321-515_321-514delinsTG
ENST00000530998.5:c.652+87_652+88delinsTG	ENSP00000435307.1:n.652+87_652+88delinsTG
NM_000378.4:c.1288+87_1288+88delinsTG	NP_000369.3:n.1288+87_1288+88delinsTG
NM_001198551.1:c.703+87_703+88delinsTG , LRG_525t2:c.703+87_703+88delinsTG	NP_001185480.1:n.703+87_703+88delinsTG
NM_001198552.1:c.652+87_652+88delinsTG	NP_001185481.1:n.652+87_652+88delinsTG
NM_024424.3:c.1339+87_1339+88delinsTG	NP_077742.2:n.1339+87_1339+88delinsTG
NM_024426.4:c.1339+87_1339+88delinsTG	NP_077744.3:n.1339+87_1339+88delinsTG
NM_000378.5:c.1303+87_1303+88delinsTG	NP_000369.4:n.1303+87_1303+88delinsTG
NM_024424.4:c.1354+87_1354+88delinsTG	NP_077742.3:n.1354+87_1354+88delinsTG
NM_024426.5:c.1354+87_1354+88delinsTG	NP_077744.4:n.1354+87_1354+88delinsTG
NM_001367854.1:c.166+87_166+88delinsTG	NP_001354783.1:n.166+87_166+88delinsTG
NR_160306.1:n.1686+87_1686+88delinsTG
NM_000378.6:c.1303+87_1303+88delinsTG	NP_000369.4:n.1303+87_1303+88delinsTG
NM_001198552.2:c.652+87_652+88delinsTG	NP_001185481.1:n.652+87_652+88delinsTG
NM_024424.5:c.1354+87_1354+88delinsTG	NP_077742.3:n.1354+87_1354+88delinsTG
NM_024426.6:c.1354+87_1354+88delinsTG MANE Select	NP_077744.4:n.1354+87_1354+88delinsTG