Canonical Allele Identifier: CA2563825404
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392606_32392607insCCCCCCCCCCCCCCCCCCCCCCCCCCCC , CM000673.2:g.32392606_32392607insCCCCCCCCCCCCCCCCCCCCCCCCCCCC GRCh38
NC_000011.9:g.32414152_32414153insCCCCCCCCCCCCCCCCCCCCCCCCCCCC , CM000673.1:g.32414152_32414153insCCCCCCCCCCCCCCCCCCCCCCCCCCCC GRCh37
NC_000011.8:g.32370728_32370729insCCCCCCCCCCCCCCCCCCCCCCCCCCCC NCBI36
NG_009272.1:g.47935_47936insGGGGGGGGGGGGGGGGGGGGGGGGGGGG , LRG_525:g.47935_47936insGGGGGGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.1303+59_1303+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000331327.5:n.1303+59_1303+60insGGG...
ENST00000379077.9:c.*538+59_*538+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000368368.5:n.*538+59_*538+60insGGG...
ENST00000379079.8:c.703+59_703+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000368370.2:n.703+59_703+60insGGGGG...
ENST00000448076.9:c.1354+59_1354+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000413452.5:n.1354+59_1354+60insGGG...
ENST00000452863.10:c.1354+59_1354+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select ENSP00000415516.5:n.1354+59_1354+60insGGG...
ENST00000526685.2:n.808+59_808+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000639563.3:c.1303+59_1303+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000492269.3:n.1303+59_1303+60insGGG...
ENST00000639907.2:n.497+59_497+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000640146.2:c.679+59_679+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000491984.2:n.679+59_679+60insGGGGG...
ENST00000650745.1:n.622_623insGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000650861.1:n.1935+59_1935+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000651459.1:c.125+59_125+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000651533.1:n.400+59_400+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000651668.1:n.291+59_291+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000651794.1:n.1197+59_1197+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000651819.1:n.279+59_279+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000652579.1:n.614+59_614+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000652724.1:n.544+59_544+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000332351.7:c.1339+59_1339+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000331327.3:n.1339+59_1339+60insGGG...
ENST00000379077.7:c.*538+59_*538+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000368368.3:n.*538+59_*538+60insGGG...
ENST00000379079.6:c.703+59_703+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000368370.2:n.703+59_703+60insGGGGG...
ENST00000448076.7:c.1339+59_1339+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000413452.3:n.1339+59_1339+60insGGG...
ENST00000452863.7:c.1288+59_1288+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000415516.3:n.1288+59_1288+60insGGG...
ENST00000527882.5:c.321-543_321-542insGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000530998.5:c.652+59_652+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000435307.1:n.652+59_652+60insGGGGG...
NM_000378.4:c.1288+59_1288+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_000369.3:n.1288+59_1288+60insGGGGGGGGG...
NM_001198551.1:c.703+59_703+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG , LRG_525t2:c.703+59_703+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001185480.1:n.703+59_703+60insGGGGGGGG...
NM_001198552.1:c.652+59_652+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001185481.1:n.652+59_652+60insGGGGGGGG...
NM_024424.3:c.1339+59_1339+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_077742.2:n.1339+59_1339+60insGGGGGGGGG...
NM_024426.4:c.1339+59_1339+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_077744.3:n.1339+59_1339+60insGGGGGGGGG...
NM_000378.5:c.1303+59_1303+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_000369.4:n.1303+59_1303+60insGGGGGGGGG...
NM_024424.4:c.1354+59_1354+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_077742.3:n.1354+59_1354+60insGGGGGGGGG...
NM_024426.5:c.1354+59_1354+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_077744.4:n.1354+59_1354+60insGGGGGGGGG...
NM_001367854.1:c.166+59_166+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001354783.1:n.166+59_166+60insGGGGGGGG...
NR_160306.1:n.1686+59_1686+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NM_000378.6:c.1303+59_1303+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_000369.4:n.1303+59_1303+60insGGGGGGGGG...
NM_001198552.2:c.652+59_652+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_001185481.1:n.652+59_652+60insGGGGGGGG...
NM_024424.5:c.1354+59_1354+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_077742.3:n.1354+59_1354+60insGGGGGGGGG...
NM_024426.6:c.1354+59_1354+60insGGGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select NP_077744.4:n.1354+59_1354+60insGGGGGGGGG...