Canonical Allele Identifier: CA1962335261

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392007A= , CM000673.2:g.32392007A=	GRCh38
NC_000011.9:g.32413553A= , CM000673.1:g.32413553A=	GRCh37
NC_000011.8:g.32370129A=	NCBI36
NG_009272.1:g.48535T= , LRG_525:g.48535T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1361T=	ENSP00000331327.5:p.Leu454=
ENST00000379077.9:c.*596T=	ENSP00000368368.5:n.*596T=
ENST00000379079.8:c.761T=	ENSP00000368370.2:p.Leu254=
ENST00000448076.9:c.1412T=	ENSP00000413452.5:p.Leu471=
ENST00000452863.10:c.1412T= MANE Select	ENSP00000415516.5:p.Leu471=
ENST00000526685.2:n.866T=
ENST00000639563.3:c.1361T=	ENSP00000492269.3:p.Leu454=
ENST00000639907.2:n.555T=
ENST00000640146.2:c.737T=	ENSP00000491984.2:p.Leu246=
ENST00000650745.1:n.1222T=
ENST00000650861.1:n.1993T=
ENST00000650986.1:n.75T=
ENST00000651459.1:c.183T=
ENST00000651533.1:n.458T=
ENST00000651668.1:n.349T=
ENST00000651794.1:n.1255T=
ENST00000651819.1:n.337T=
ENST00000652579.1:n.672T=
ENST00000652724.1:n.602T=
ENST00000332351.7:c.1397T=	ENSP00000331327.3:p.Leu466=
ENST00000379077.7:c.*596T=	ENSP00000368368.3:n.*596T=
ENST00000379079.6:c.761T=	ENSP00000368370.2:p.Leu254=
ENST00000448076.7:c.1397T=	ENSP00000413452.3:p.Leu466=
ENST00000452863.7:c.1346T=	ENSP00000415516.3:p.Leu449=
ENST00000527882.5:c.378T=
ENST00000530998.5:c.710T=	ENSP00000435307.1:p.Leu237=
NM_000378.4:c.1346T=	NP_000369.3:p.Leu449=
NM_001198551.1:c.761T= , LRG_525t2:c.761T=	NP_001185480.1:p.Leu254=
NM_001198552.1:c.710T=	NP_001185481.1:p.Leu237=
NM_024424.3:c.1397T=	NP_077742.2:p.Leu466=
NM_024426.4:c.1397T=	NP_077744.3:p.Leu466=
NM_000378.5:c.1361T=	NP_000369.4:p.Leu454=
NM_024424.4:c.1412T=	NP_077742.3:p.Leu471=
NM_024426.5:c.1412T=	NP_077744.4:p.Leu471=
NM_001367854.1:c.224T=	NP_001354783.1:p.Leu75=
NR_160306.1:n.1744T=
NM_000378.6:c.1361T=	NP_000369.4:p.Leu454=
NM_001198552.2:c.710T=	NP_001185481.1:p.Leu237=
NM_024424.5:c.1412T=	NP_077742.3:p.Leu471=
NM_024426.6:c.1412T= MANE Select	NP_077744.4:p.Leu471=