Canonical Allele Identifier: CA1962323554

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32428507C= , CM000673.2:g.32428507C=	GRCh38
NC_000011.9:g.32450053C= , CM000673.1:g.32450053C=	GRCh37
NC_000011.8:g.32406629C=	NCBI36
NG_009272.1:g.12035G= , LRG_525:g.12035G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.774G=	ENSP00000331327.5:p.Gln258=
ENST00000379077.9:c.774G=	ENSP00000368368.5:p.Gln258=
ENST00000379079.8:c.123G=	ENSP00000368370.2:p.Gln41=
ENST00000448076.9:c.774G=	ENSP00000413452.5:p.Gln258=
ENST00000452863.10:c.774G= MANE Select	ENSP00000415516.5:p.Gln258=
ENST00000639563.3:c.774G=	ENSP00000492269.3:p.Gln258=
ENST00000640146.2:c.150G=	ENSP00000491984.2:p.Gln50=
ENST00000332351.7:c.759G=	ENSP00000331327.3:p.Gln253=
ENST00000379077.7:c.759G=	ENSP00000368368.3:p.Gln253=
ENST00000379079.6:c.123G=	ENSP00000368370.2:p.Gln41=
ENST00000448076.7:c.759G=	ENSP00000413452.3:p.Gln253=
ENST00000452863.7:c.759G=	ENSP00000415516.3:p.Gln253=
ENST00000527775.1:c.12G=	ENSP00000435351.1:p.Gln4=
ENST00000530998.5:c.123G=	ENSP00000435307.1:p.Gln41=
NM_000378.4:c.759G=	NP_000369.3:p.Gln253=
NM_001198551.1:c.123G= , LRG_525t2:c.123G=	NP_001185480.1:p.Gln41=
NM_001198552.1:c.123G=	NP_001185481.1:p.Gln41=
NM_024424.3:c.759G=	NP_077742.2:p.Gln253=
NM_024426.4:c.759G=	NP_077744.3:p.Gln253=
NM_000378.5:c.774G=	NP_000369.4:p.Gln258=
NM_024424.4:c.774G=	NP_077742.3:p.Gln258=
NM_024426.5:c.774G=	NP_077744.4:p.Gln258=
NR_160306.1:n.953G=
NM_000378.6:c.774G=	NP_000369.4:p.Gln258=
NM_001198552.2:c.123G=	NP_001185481.1:p.Gln41=
NM_024424.5:c.774G=	NP_077742.3:p.Gln258=
NM_024426.6:c.774G= MANE Select	NP_077744.4:p.Gln258=