Canonical Allele Identifier: CA1962335280

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392031C= , CM000673.2:g.32392031C=	GRCh38
NC_000011.9:g.32413577C= , CM000673.1:g.32413577C=	GRCh37
NC_000011.8:g.32370153C=	NCBI36
NG_009272.1:g.48511G= , LRG_525:g.48511G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1337G=	ENSP00000331327.5:p.Arg446=
ENST00000379077.9:c.*572G=	ENSP00000368368.5:n.*572G=
ENST00000379079.8:c.737G=	ENSP00000368370.2:p.Arg246=
ENST00000448076.9:c.1388G=	ENSP00000413452.5:p.Arg463=
ENST00000452863.10:c.1388G= MANE Select	ENSP00000415516.5:p.Arg463=
ENST00000526685.2:n.842G=
ENST00000639563.3:c.1337G=	ENSP00000492269.3:p.Arg446=
ENST00000639907.2:n.531G=
ENST00000640146.2:c.713G=	ENSP00000491984.2:p.Arg238=
ENST00000650745.1:n.1198G=
ENST00000650861.1:n.1969G=
ENST00000650986.1:n.51G=
ENST00000651459.1:c.159G=
ENST00000651533.1:n.434G=
ENST00000651668.1:n.325G=
ENST00000651794.1:n.1231G=
ENST00000651819.1:n.313G=
ENST00000652579.1:n.648G=
ENST00000652724.1:n.578G=
ENST00000332351.7:c.1373G=	ENSP00000331327.3:p.Arg458=
ENST00000379077.7:c.*572G=	ENSP00000368368.3:n.*572G=
ENST00000379079.6:c.737G=	ENSP00000368370.2:p.Arg246=
ENST00000448076.7:c.1373G=	ENSP00000413452.3:p.Arg458=
ENST00000452863.7:c.1322G=	ENSP00000415516.3:p.Arg441=
ENST00000527882.5:c.354G=
ENST00000530998.5:c.686G=	ENSP00000435307.1:p.Arg229=
NM_000378.4:c.1322G=	NP_000369.3:p.Arg441=
NM_001198551.1:c.737G= , LRG_525t2:c.737G=	NP_001185480.1:p.Arg246=
NM_001198552.1:c.686G=	NP_001185481.1:p.Arg229=
NM_024424.3:c.1373G=	NP_077742.2:p.Arg458=
NM_024426.4:c.1373G=	NP_077744.3:p.Arg458=
NM_000378.5:c.1337G=	NP_000369.4:p.Arg446=
NM_024424.4:c.1388G=	NP_077742.3:p.Arg463=
NM_024426.5:c.1388G=	NP_077744.4:p.Arg463=
NM_001367854.1:c.200G=	NP_001354783.1:p.Arg67=
NR_160306.1:n.1720G=
NM_000378.6:c.1337G=	NP_000369.4:p.Arg446=
NM_001198552.2:c.686G=	NP_001185481.1:p.Arg229=
NM_024424.5:c.1388G=	NP_077742.3:p.Arg463=
NM_024426.6:c.1388G= MANE Select	NP_077744.4:p.Arg463=