Canonical Allele Identifier: CA1962335274
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392024G= , CM000673.2:g.32392024G= GRCh38
NC_000011.9:g.32413570G= , CM000673.1:g.32413570G= GRCh37
NC_000011.8:g.32370146G= NCBI36
NG_009272.1:g.48518C= , LRG_525:g.48518C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1344C= ENSP00000331327.5:p.Phe448=
ENST00000379077.9:c.*579C= ENSP00000368368.5:n.*579C=
ENST00000379079.8:c.744C= ENSP00000368370.2:p.Phe248=
ENST00000448076.9:c.1395C= ENSP00000413452.5:p.Phe465=
ENST00000452863.10:c.1395C= MANE Select ENSP00000415516.5:p.Phe465=
ENST00000526685.2:n.849C=
ENST00000639563.3:c.1344C= ENSP00000492269.3:p.Phe448=
ENST00000639907.2:n.538C=
ENST00000640146.2:c.720C= ENSP00000491984.2:p.Phe240=
ENST00000650745.1:n.1205C=
ENST00000650861.1:n.1976C=
ENST00000650986.1:n.58C=
ENST00000651459.1:c.166C=
ENST00000651533.1:n.441C=
ENST00000651668.1:n.332C=
ENST00000651794.1:n.1238C=
ENST00000651819.1:n.320C=
ENST00000652579.1:n.655C=
ENST00000652724.1:n.585C=
ENST00000332351.7:c.1380C= ENSP00000331327.3:p.Phe460=
ENST00000379077.7:c.*579C= ENSP00000368368.3:n.*579C=
ENST00000379079.6:c.744C= ENSP00000368370.2:p.Phe248=
ENST00000448076.7:c.1380C= ENSP00000413452.3:p.Phe460=
ENST00000452863.7:c.1329C= ENSP00000415516.3:p.Phe443=
ENST00000527882.5:c.361C=
ENST00000530998.5:c.693C= ENSP00000435307.1:p.Phe231=
NM_000378.4:c.1329C= NP_000369.3:p.Phe443=
NM_001198551.1:c.744C= , LRG_525t2:c.744C= NP_001185480.1:p.Phe248=
NM_001198552.1:c.693C= NP_001185481.1:p.Phe231=
NM_024424.3:c.1380C= NP_077742.2:p.Phe460=
NM_024426.4:c.1380C= NP_077744.3:p.Phe460=
NM_000378.5:c.1344C= NP_000369.4:p.Phe448=
NM_024424.4:c.1395C= NP_077742.3:p.Phe465=
NM_024426.5:c.1395C= NP_077744.4:p.Phe465=
NM_001367854.1:c.207C= NP_001354783.1:p.Phe69=
NR_160306.1:n.1727C=
NM_000378.6:c.1344C= NP_000369.4:p.Phe448=
NM_001198552.2:c.693C= NP_001185481.1:p.Phe231=
NM_024424.5:c.1395C= NP_077742.3:p.Phe465=
NM_024426.6:c.1395C= MANE Select NP_077744.4:p.Phe465=