Canonical Allele Identifier: CA2844606162
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32391936_32391946dup , CM000673.2:g.32391936_32391946dup GRCh38
NC_000011.9:g.32413482_32413492dup , CM000673.1:g.32413482_32413492dup GRCh37
NC_000011.8:g.32370058_32370068dup NCBI36
NG_009272.1:g.48601_48611dup , LRG_525:g.48601_48611dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1387+40_1387+50dup ENSP00000331327.5:n.1387+40_1387+50dup
ENST00000379077.9:c.*631+31_*631+41dup ENSP00000368368.5:n.*631+31_*631+41dup
ENST00000379079.8:c.787+40_787+50dup ENSP00000368370.2:n.787+40_787+50dup
ENST00000448076.9:c.1438+40_1438+50dup ENSP00000413452.5:n.1438+40_1438+50dup
ENST00000452863.10:c.1447+31_1447+41dup MANE Select ENSP00000415516.5:n.1447+31_1447+41dup
ENST00000526685.2:n.892+40_892+50dup
ENST00000639563.3:c.1396+31_1396+41dup ENSP00000492269.3:n.1396+31_1396+41dup
ENST00000639907.2:n.581+40_581+50dup
ENST00000640146.2:c.772+31_772+41dup ENSP00000491984.2:n.772+31_772+41dup
ENST00000650745.1:n.1257+31_1257+41dup
ENST00000650861.1:n.2019+40_2019+50dup
ENST00000650986.1:n.110+31_110+41dup
ENST00000651459.1:c.218+31_218+41dup
ENST00000651533.1:n.484+40_484+50dup
ENST00000651668.1:n.384+31_384+41dup
ENST00000651794.1:n.1290+31_1290+41dup
ENST00000651819.1:n.372+31_372+41dup
ENST00000652579.1:n.707+31_707+41dup
ENST00000652724.1:n.637+31_637+41dup
ENST00000332351.7:c.1432+31_1432+41dup ENSP00000331327.3:n.1432+31_1432+41dup
ENST00000379077.7:c.*631+31_*631+41dup ENSP00000368368.3:n.*631+31_*631+41dup
ENST00000379079.6:c.787+40_787+50dup ENSP00000368370.2:n.787+40_787+50dup
ENST00000448076.7:c.1423+40_1423+50dup ENSP00000413452.3:n.1423+40_1423+50dup
ENST00000452863.7:c.1372+40_1372+50dup ENSP00000415516.3:n.1372+40_1372+50dup
ENST00000527882.5:c.413+31_413+41dup
ENST00000530998.5:c.745+31_745+41dup ENSP00000435307.1:n.745+31_745+41dup
NM_000378.4:c.1372+40_1372+50dup NP_000369.3:n.1372+40_1372+50dup
NM_001198551.1:c.787+40_787+50dup , LRG_525t2:c.787+40_787+50dup NP_001185480.1:n.787+40_787+50dup
NM_001198552.1:c.745+31_745+41dup NP_001185481.1:n.745+31_745+41dup
NM_024424.3:c.1423+40_1423+50dup NP_077742.2:n.1423+40_1423+50dup
NM_024426.4:c.1432+31_1432+41dup NP_077744.3:n.1432+31_1432+41dup
NM_000378.5:c.1387+40_1387+50dup NP_000369.4:n.1387+40_1387+50dup
NM_024424.4:c.1438+40_1438+50dup NP_077742.3:n.1438+40_1438+50dup
NM_024426.5:c.1447+31_1447+41dup NP_077744.4:n.1447+31_1447+41dup
NM_001367854.1:c.259+31_259+41dup NP_001354783.1:n.259+31_259+41dup
NR_160306.1:n.1779+31_1779+41dup
NM_000378.6:c.1387+40_1387+50dup NP_000369.4:n.1387+40_1387+50dup
NM_001198552.2:c.745+31_745+41dup NP_001185481.1:n.745+31_745+41dup
NM_024424.5:c.1438+40_1438+50dup NP_077742.3:n.1438+40_1438+50dup
NM_024426.6:c.1447+31_1447+41dup MANE Select NP_077744.4:n.1447+31_1447+41dup