Canonical Allele Identifier: CA473568259

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32416498C>T , CM000673.2:g.32416498C>T	GRCh38
NC_000011.9:g.32438044C>T , CM000673.1:g.32438044C>T	GRCh37
NC_000011.8:g.32394620C>T	NCBI36
NG_009272.1:g.24044G>A , LRG_525:g.24044G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.965+1079G>A	ENSP00000331327.5:n.965+1079G>A
ENST00000379077.9:c.*192G>A	ENSP00000368368.5:n.*192G>A
ENST00000379079.8:c.357G>A	ENSP00000368370.2:p.Gly119=
ENST00000448076.9:c.1008G>A	ENSP00000413452.5:p.Gly336=
ENST00000452863.10:c.1008G>A MANE Select	ENSP00000415516.5:p.Gly336=
ENST00000639563.3:c.965+1079G>A	ENSP00000492269.3:n.965+1079G>A
ENST00000640146.2:c.341+1079G>A	ENSP00000491984.2:n.341+1079G>A
ENST00000651794.1:n.751G>A
ENST00000332351.7:c.993G>A	ENSP00000331327.3:p.Gly331=
ENST00000379077.7:c.*192G>A	ENSP00000368368.3:n.*192G>A
ENST00000379079.6:c.357G>A	ENSP00000368370.2:p.Gly119=
ENST00000448076.7:c.993G>A	ENSP00000413452.3:p.Gly331=
ENST00000452863.7:c.950+1079G>A	ENSP00000415516.3:n.950+1079G>A
ENST00000527775.1:c.246G>A	ENSP00000435351.1:p.Gly82=
ENST00000527882.5:c.64G>A
ENST00000530998.5:c.314+1079G>A	ENSP00000435307.1:n.314+1079G>A
NM_000378.4:c.950+1079G>A	NP_000369.3:n.950+1079G>A
NM_001198551.1:c.357G>A , LRG_525t2:c.357G>A	NP_001185480.1:p.Gly119=
NM_001198552.1:c.314+1079G>A	NP_001185481.1:n.314+1079G>A
NM_024424.3:c.993G>A	NP_077742.2:p.Gly331=
NM_024426.4:c.993G>A	NP_077744.3:p.Gly331=
NM_000378.5:c.965+1079G>A	NP_000369.4:n.965+1079G>A
NM_024424.4:c.1008G>A	NP_077742.3:p.Gly336=
NM_024426.5:c.1008G>A	NP_077744.4:p.Gly336=
NR_160306.1:n.1340G>A
NM_000378.6:c.965+1079G>A	NP_000369.4:n.965+1079G>A
NM_001198552.2:c.314+1079G>A	NP_001185481.1:n.314+1079G>A
NM_024424.5:c.1008G>A	NP_077742.3:p.Gly336=
NM_024426.6:c.1008G>A MANE Select	NP_077744.4:p.Gly336=