Canonical Allele Identifier: CA1962310466
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32387875C= , CM000673.2:g.32387875C= GRCh38
NC_000011.9:g.32409421C= , CM000673.1:g.32409421C= GRCh37
NC_000011.8:g.32365997C= NCBI36
NG_009272.1:g.52667G= , LRG_525:g.52667G=

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.*1183G= ENSP00000331327.5:n.*1183G=
ENST00000379077.9:c.*1936G= ENSP00000368368.5:n.*1936G=
ENST00000379079.8:c.*1183G= ENSP00000368370.2:n.*1183G=
ENST00000452863.10:c.*1183G= MANE Select ENSP00000415516.5:n.*1183G=
ENST00000332351.7:c.*1183G= ENSP00000331327.3:n.*1183G=
ENST00000379077.7:c.*1936G= ENSP00000368368.3:n.*1936G=
ENST00000379079.6:c.*1183G= ENSP00000368370.2:n.*1183G=
ENST00000452863.7:c.2677G= ENSP00000415516.3:n.2677G=
ENST00000530998.5:c.*1183G= ENSP00000435307.1:n.*1183G=
NM_000378.4:c.*1183G= NP_000369.3:n.*1183G=
NM_001198551.1:c.*1183G= , LRG_525t2:c.*1183G= NP_001185480.1:n.*1183G=
NM_001198552.1:c.*1183G= NP_001185481.1:n.*1183G=
NM_024424.3:c.*1183G= NP_077742.2:n.*1183G=
NM_024426.4:c.*1183G= NP_077744.3:n.*1183G=
NM_000378.5:c.*1183G= NP_000369.4:n.*1183G=
NM_024424.4:c.*1183G= NP_077742.3:n.*1183G=
NM_024426.5:c.*1183G= NP_077744.4:n.*1183G=
NM_001367854.1:c.*1183G= NP_001354783.1:n.*1183G=
NR_160306.1:n.3084G=
NM_000378.6:c.*1183G= NP_000369.4:n.*1183G=
NM_001198552.2:c.*1183G= NP_001185481.1:n.*1183G=
NM_024424.5:c.*1183G= NP_077742.3:n.*1183G=
NM_024426.6:c.*1183G= MANE Select NP_077744.4:n.*1183G=