Canonical Allele Identifier: CA1962318452

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417623C= , CM000673.2:g.32417623C=	GRCh38
NC_000011.9:g.32439169C= , CM000673.1:g.32439169C=	GRCh37
NC_000011.8:g.32395745C=	NCBI36
NG_009272.1:g.22919G= , LRG_525:g.22919G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.919G=	ENSP00000331327.5:p.Glu307=
ENST00000379077.9:c.919G=	ENSP00000368368.5:p.Glu307=
ENST00000379079.8:c.268G=	ENSP00000368370.2:p.Glu90=
ENST00000448076.9:c.919G=	ENSP00000413452.5:p.Glu307=
ENST00000452863.10:c.919G= MANE Select	ENSP00000415516.5:p.Glu307=
ENST00000639563.3:c.919G=	ENSP00000492269.3:p.Glu307=
ENST00000640146.2:c.295G=	ENSP00000491984.2:p.Glu99=
ENST00000332351.7:c.904G=	ENSP00000331327.3:p.Glu302=
ENST00000379077.7:c.904G=	ENSP00000368368.3:p.Glu302=
ENST00000379079.6:c.268G=	ENSP00000368370.2:p.Glu90=
ENST00000448076.7:c.904G=	ENSP00000413452.3:p.Glu302=
ENST00000452863.7:c.904G=	ENSP00000415516.3:p.Glu302=
ENST00000527775.1:c.157G=	ENSP00000435351.1:p.Glu53=
ENST00000530998.5:c.268G=	ENSP00000435307.1:p.Glu90=
NM_000378.4:c.904G=	NP_000369.3:p.Glu302=
NM_001198551.1:c.268G= , LRG_525t2:c.268G=	NP_001185480.1:p.Glu90=
NM_001198552.1:c.268G=	NP_001185481.1:p.Glu90=
NM_024424.3:c.904G=	NP_077742.2:p.Glu302=
NM_024426.4:c.904G=	NP_077744.3:p.Glu302=
NM_000378.5:c.919G=	NP_000369.4:p.Glu307=
NM_024424.4:c.919G=	NP_077742.3:p.Glu307=
NM_024426.5:c.919G=	NP_077744.4:p.Glu307=
NR_160306.1:n.1098G=
NM_000378.6:c.919G=	NP_000369.4:p.Glu307=
NM_001198552.2:c.268G=	NP_001185481.1:p.Glu90=
NM_024424.5:c.919G=	NP_077742.3:p.Glu307=
NM_024426.6:c.919G= MANE Select	NP_077744.4:p.Glu307=