Canonical Allele Identifier: CA065543
Gene: WT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32428521G>T , CM000673.2:g.32428521G>T GRCh38
NC_000011.9:g.32450067G>T , CM000673.1:g.32450067G>T GRCh37
NC_000011.8:g.32406643G>T NCBI36
NG_009272.1:g.12021C>A , LRG_525:g.12021C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.760C>A ENSP00000331327.5:p.Pro254Thr
ENST00000379077.9:c.760C>A ENSP00000368368.5:p.Pro254Thr
ENST00000379079.8:c.109C>A ENSP00000368370.2:p.Pro37Thr
ENST00000448076.9:c.760C>A ENSP00000413452.5:p.Pro254Thr
ENST00000452863.10:c.760C>A MANE Select ENSP00000415516.5:p.Pro254Thr
ENST00000639563.3:c.760C>A ENSP00000492269.3:p.Pro254Thr
ENST00000640146.2:c.136C>A ENSP00000491984.2:p.Pro46Thr
ENST00000332351.7:c.745C>A ENSP00000331327.3:p.Pro249Thr
ENST00000379077.7:c.745C>A ENSP00000368368.3:p.Pro249Thr
ENST00000379079.6:c.109C>A ENSP00000368370.2:p.Pro37Thr
ENST00000448076.7:c.745C>A ENSP00000413452.3:p.Pro249Thr
ENST00000452863.7:c.745C>A ENSP00000415516.3:p.Pro249Thr
ENST00000527775.1:c.-3C>A ENSP00000435351.1:n.-3C>A
ENST00000530998.5:c.109C>A ENSP00000435307.1:p.Pro37Thr
NM_000378.4:c.745C>A NP_000369.3:p.Pro249Thr
NM_001198551.1:c.109C>A , LRG_525t2:c.109C>A NP_001185480.1:p.Pro37Thr
NM_001198552.1:c.109C>A NP_001185481.1:p.Pro37Thr
NM_024424.3:c.745C>A NP_077742.2:p.Pro249Thr
NM_024426.4:c.745C>A NP_077744.3:p.Pro249Thr
NM_000378.5:c.760C>A NP_000369.4:p.Pro254Thr
NM_024424.4:c.760C>A NP_077742.3:p.Pro254Thr
NM_024426.5:c.760C>A NP_077744.4:p.Pro254Thr
NR_160306.1:n.939C>A
NM_000378.6:c.760C>A NP_000369.4:p.Pro254Thr
NM_001198552.2:c.109C>A NP_001185481.1:p.Pro37Thr
NM_024424.5:c.760C>A NP_077742.3:p.Pro254Thr
NM_024426.6:c.760C>A MANE Select NP_077744.4:p.Pro254Thr
Search 100 bp 5'
Search 100 bp 3'