Canonical Allele Identifier: CA1962335540
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392672G= , CM000673.2:g.32392672G= GRCh38
NC_000011.9:g.32414218G= , CM000673.1:g.32414218G= GRCh37
NC_000011.8:g.32370794G= NCBI36
NG_009272.1:g.47870C= , LRG_525:g.47870C=

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.1297C= ENSP00000331327.5:p.His433=
ENST00000379077.9:c.*532C= ENSP00000368368.5:n.*532C=
ENST00000379079.8:c.697C= ENSP00000368370.2:p.His233=
ENST00000448076.9:c.1348C= ENSP00000413452.5:p.His450=
ENST00000452863.10:c.1348C= MANE Select ENSP00000415516.5:p.His450=
ENST00000526685.2:n.802C=
ENST00000639563.3:c.1297C= ENSP00000492269.3:p.His433=
ENST00000639907.2:n.491C=
ENST00000640146.2:c.673C= ENSP00000491984.2:p.His225=
ENST00000650745.1:n.557C=
ENST00000650861.1:n.1929C=
ENST00000651459.1:c.119C=
ENST00000651533.1:n.394C=
ENST00000651668.1:n.285C=
ENST00000651794.1:n.1191C=
ENST00000651819.1:n.273C=
ENST00000652579.1:n.608C=
ENST00000652724.1:n.538C=
ENST00000332351.7:c.1333C= ENSP00000331327.3:p.His445=
ENST00000379077.7:c.*532C= ENSP00000368368.3:n.*532C=
ENST00000379079.6:c.697C= ENSP00000368370.2:p.His233=
ENST00000448076.7:c.1333C= ENSP00000413452.3:p.His445=
ENST00000452863.7:c.1282C= ENSP00000415516.3:p.His428=
ENST00000527882.5:c.321-608C=
ENST00000530998.5:c.646C= ENSP00000435307.1:p.His216=
NM_000378.4:c.1282C= NP_000369.3:p.His428=
NM_001198551.1:c.697C= , LRG_525t2:c.697C= NP_001185480.1:p.His233=
NM_001198552.1:c.646C= NP_001185481.1:p.His216=
NM_024424.3:c.1333C= NP_077742.2:p.His445=
NM_024426.4:c.1333C= NP_077744.3:p.His445=
NM_000378.5:c.1297C= NP_000369.4:p.His433=
NM_024424.4:c.1348C= NP_077742.3:p.His450=
NM_024426.5:c.1348C= NP_077744.4:p.His450=
NM_001367854.1:c.160C= NP_001354783.1:p.His54=
NR_160306.1:n.1680C=
NM_000378.6:c.1297C= NP_000369.4:p.His433=
NM_001198552.2:c.646C= NP_001185481.1:p.His216=
NM_024424.5:c.1348C= NP_077742.3:p.His450=
NM_024426.6:c.1348C= MANE Select NP_077744.4:p.His450=