Canonical Allele Identifier: CA1962335543
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392679T= , CM000673.2:g.32392679T= GRCh38
NC_000011.9:g.32414225T= , CM000673.1:g.32414225T= GRCh37
NC_000011.8:g.32370801T= NCBI36
NG_009272.1:g.47863A= , LRG_525:g.47863A=

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.1290A= ENSP00000331327.5:p.Gln430=
ENST00000379077.9:c.*525A= ENSP00000368368.5:n.*525A=
ENST00000379079.8:c.690A= ENSP00000368370.2:p.Gln230=
ENST00000448076.9:c.1341A= ENSP00000413452.5:p.Gln447=
ENST00000452863.10:c.1341A= MANE Select ENSP00000415516.5:p.Gln447=
ENST00000526685.2:n.795A=
ENST00000639563.3:c.1290A= ENSP00000492269.3:p.Gln430=
ENST00000639907.2:n.484A=
ENST00000640146.2:c.666A= ENSP00000491984.2:p.Gln222=
ENST00000650745.1:n.550A=
ENST00000650861.1:n.1922A=
ENST00000651459.1:c.112A=
ENST00000651533.1:n.387A=
ENST00000651668.1:n.278A=
ENST00000651794.1:n.1184A=
ENST00000651819.1:n.266A=
ENST00000652579.1:n.601A=
ENST00000652724.1:n.531A=
ENST00000332351.7:c.1326A= ENSP00000331327.3:p.Gln442=
ENST00000379077.7:c.*525A= ENSP00000368368.3:n.*525A=
ENST00000379079.6:c.690A= ENSP00000368370.2:p.Gln230=
ENST00000448076.7:c.1326A= ENSP00000413452.3:p.Gln442=
ENST00000452863.7:c.1275A= ENSP00000415516.3:p.Gln425=
ENST00000527882.5:c.321-615A=
ENST00000530998.5:c.639A= ENSP00000435307.1:p.Gln213=
NM_000378.4:c.1275A= NP_000369.3:p.Gln425=
NM_001198551.1:c.690A= , LRG_525t2:c.690A= NP_001185480.1:p.Gln230=
NM_001198552.1:c.639A= NP_001185481.1:p.Gln213=
NM_024424.3:c.1326A= NP_077742.2:p.Gln442=
NM_024426.4:c.1326A= NP_077744.3:p.Gln442=
NM_000378.5:c.1290A= NP_000369.4:p.Gln430=
NM_024424.4:c.1341A= NP_077742.3:p.Gln447=
NM_024426.5:c.1341A= NP_077744.4:p.Gln447=
NM_001367854.1:c.153A= NP_001354783.1:p.Gln51=
NR_160306.1:n.1673A=
NM_000378.6:c.1290A= NP_000369.4:p.Gln430=
NM_001198552.2:c.639A= NP_001185481.1:p.Gln213=
NM_024424.5:c.1341A= NP_077742.3:p.Gln447=
NM_024426.6:c.1341A= MANE Select NP_077744.4:p.Gln447=