Canonical Allele Identifier: CA1962335555

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392739C= , CM000673.2:g.32392739C=	GRCh38
NC_000011.9:g.32414285C= , CM000673.1:g.32414285C=	GRCh37
NC_000011.8:g.32370861C=	NCBI36
NG_009272.1:g.47803G= , LRG_525:g.47803G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1230G=	ENSP00000331327.5:p.Gln410=
ENST00000379077.9:c.*465G=	ENSP00000368368.5:n.*465G=
ENST00000379079.8:c.630G=	ENSP00000368370.2:p.Gln210=
ENST00000448076.9:c.1281G=	ENSP00000413452.5:p.Gln427=
ENST00000452863.10:c.1281G= MANE Select	ENSP00000415516.5:p.Gln427=
ENST00000526685.2:n.735G=
ENST00000639563.3:c.1230G=	ENSP00000492269.3:p.Gln410=
ENST00000639907.2:n.424G=
ENST00000640146.2:c.606G=	ENSP00000491984.2:p.Gln202=
ENST00000650745.1:n.490G=
ENST00000650861.1:n.1862G=
ENST00000651459.1:c.52G=
ENST00000651533.1:n.327G=
ENST00000651668.1:n.218G=
ENST00000651794.1:n.1124G=
ENST00000651819.1:n.206G=
ENST00000652579.1:n.541G=
ENST00000652724.1:n.471G=
ENST00000332351.7:c.1266G=	ENSP00000331327.3:p.Gln422=
ENST00000379077.7:c.*465G=	ENSP00000368368.3:n.*465G=
ENST00000379079.6:c.630G=	ENSP00000368370.2:p.Gln210=
ENST00000448076.7:c.1266G=	ENSP00000413452.3:p.Gln422=
ENST00000452863.7:c.1215G=	ENSP00000415516.3:p.Gln405=
ENST00000527882.5:c.321-675G=
ENST00000530998.5:c.579G=	ENSP00000435307.1:p.Gln193=
NM_000378.4:c.1215G=	NP_000369.3:p.Gln405=
NM_001198551.1:c.630G= , LRG_525t2:c.630G=	NP_001185480.1:p.Gln210=
NM_001198552.1:c.579G=	NP_001185481.1:p.Gln193=
NM_024424.3:c.1266G=	NP_077742.2:p.Gln422=
NM_024426.4:c.1266G=	NP_077744.3:p.Gln422=
NM_000378.5:c.1230G=	NP_000369.4:p.Gln410=
NM_024424.4:c.1281G=	NP_077742.3:p.Gln427=
NM_024426.5:c.1281G=	NP_077744.4:p.Gln427=
NM_001367854.1:c.93G=	NP_001354783.1:p.Gln31=
NR_160306.1:n.1613G=
NM_000378.6:c.1230G=	NP_000369.4:p.Gln410=
NM_001198552.2:c.579G=	NP_001185481.1:p.Gln193=
NM_024424.5:c.1281G=	NP_077742.3:p.Gln427=
NM_024426.6:c.1281G= MANE Select	NP_077744.4:p.Gln427=