Canonical Allele Identifier: CA064686

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32389064C>T , CM000673.2:g.32389064C>T	GRCh38
NC_000011.9:g.32410610C>T , CM000673.1:g.32410610C>T	GRCh37
NC_000011.8:g.32367186C>T	NCBI36
NG_009272.1:g.51478G>A , LRG_525:g.51478G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024426.6:c.1563G>A MANE Select	NP_077744.4:p.Ala521=
ENST00000452863.10:c.1563G>A MANE Select	ENSP00000415516.5:p.Ala521=
NM_000378.4:c.1488G>A	NP_000369.3:p.Ala496=
NM_000378.5:c.1503G>A	NP_000369.4:p.Ala501=
NM_000378.6:c.1503G>A	NP_000369.4:p.Ala501=
NM_001198551.1:c.903G>A , LRG_525t2:c.903G>A	NP_001185480.1:p.Ala301=
NM_001198552.1:c.861G>A	NP_001185481.1:p.Ala287=
NM_001198552.2:c.861G>A	NP_001185481.1:p.Ala287=
NM_001367854.1:c.375G>A	NP_001354783.1:p.Ala125=
NM_024424.3:c.1539G>A	NP_077742.2:p.Ala513=
NM_024424.4:c.1554G>A	NP_077742.3:p.Ala518=
NM_024424.5:c.1554G>A	NP_077742.3:p.Ala518=
NM_024426.4:c.1548G>A	NP_077744.3:p.Ala516=
NM_024426.5:c.1563G>A	NP_077744.4:p.Ala521=
NR_160306.1:n.1895G>A
ENST00000332351.7:c.1548G>A	ENSP00000331327.3:p.Ala516=
ENST00000332351.9:c.1503G>A	ENSP00000331327.5:p.Ala501=
ENST00000379077.7:c.*747G>A	ENSP00000368368.3:n.*747G>A
ENST00000379077.9:c.*747G>A	ENSP00000368368.5:n.*747G>A
ENST00000379079.6:c.903G>A	ENSP00000368370.2:p.Ala301=
ENST00000379079.8:c.903G>A	ENSP00000368370.2:p.Ala301=
ENST00000448076.7:c.1539G>A	ENSP00000413452.3:p.Ala513=
ENST00000448076.9:c.1554G>A	ENSP00000413452.5:p.Ala518=
ENST00000452863.7:c.1488G>A	ENSP00000415516.3:p.Ala496=
ENST00000527882.5:c.529G>A
ENST00000530998.5:c.861G>A	ENSP00000435307.1:p.Ala287=
ENST00000639563.3:c.1512G>A	ENSP00000492269.3:p.Ala504=
ENST00000639907.2:n.697G>A
ENST00000640146.2:c.888G>A	ENSP00000491984.2:p.Ala296=
ENST00000650745.1:n.1373G>A
ENST00000650861.1:n.2135G>A
ENST00000650986.1:n.226G>A
ENST00000651459.1:c.334G>A
ENST00000651533.1:n.600G>A
ENST00000651668.1:n.500G>A
ENST00000651794.1:n.1406G>A
ENST00000651819.1:n.488G>A
ENST00000652579.1:n.823G>A
ENST00000652724.1:n.753G>A