Canonical Allele Identifier: CA1962340433

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399977G= , CM000673.2:g.32399977G=	GRCh38
NC_000011.9:g.32421523G= , CM000673.1:g.32421523G=	GRCh37
NC_000011.8:g.32378099G=	NCBI36
NG_009272.1:g.40565C= , LRG_525:g.40565C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1033C=	ENSP00000331327.5:p.His345=
ENST00000379077.9:c.*268C=	ENSP00000368368.5:n.*268C=
ENST00000379079.8:c.433C=	ENSP00000368370.2:p.His145=
ENST00000448076.9:c.1084C=	ENSP00000413452.5:p.His362=
ENST00000452863.10:c.1084C= MANE Select	ENSP00000415516.5:p.His362=
ENST00000526685.2:n.538C=
ENST00000639563.3:c.1033C=	ENSP00000492269.3:p.His345=
ENST00000639907.2:n.227C=
ENST00000640146.2:c.409C=	ENSP00000491984.2:p.His137=
ENST00000651459.1:c.6C=
ENST00000651794.1:n.827C=
ENST00000652579.1:n.244C=
ENST00000652724.1:n.274C=
ENST00000332351.7:c.1069C=	ENSP00000331327.3:p.His357=
ENST00000379077.7:c.*268C=	ENSP00000368368.3:n.*268C=
ENST00000379079.6:c.433C=	ENSP00000368370.2:p.His145=
ENST00000448076.7:c.1069C=	ENSP00000413452.3:p.His357=
ENST00000452863.7:c.1018C=	ENSP00000415516.3:p.His340=
ENST00000526685.1:c.-105C=	ENSP00000436292.1:n.-105C=
ENST00000527775.1:c.322C=	ENSP00000435351.1:p.His108=
ENST00000527882.5:c.140C=
ENST00000530998.5:c.382C=	ENSP00000435307.1:p.His128=
NM_000378.4:c.1018C=	NP_000369.3:p.His340=
NM_001198551.1:c.433C= , LRG_525t2:c.433C=	NP_001185480.1:p.His145=
NM_001198552.1:c.382C=	NP_001185481.1:p.His128=
NM_024424.3:c.1069C=	NP_077742.2:p.His357=
NM_024426.4:c.1069C=	NP_077744.3:p.His357=
NM_000378.5:c.1033C=	NP_000369.4:p.His345=
NM_024424.4:c.1084C=	NP_077742.3:p.His362=
NM_024426.5:c.1084C=	NP_077744.4:p.His362=
NM_001367854.1:c.-105C=	NP_001354783.1:n.-105C=
NR_160306.1:n.1416C=
NM_000378.6:c.1033C=	NP_000369.4:p.His345=
NM_001198552.2:c.382C=	NP_001185481.1:p.His128=
NM_024424.5:c.1084C=	NP_077742.3:p.His362=
NM_024426.6:c.1084C= MANE Select	NP_077744.4:p.His362=