Canonical Allele Identifier: CA379960494

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32400023G>T , CM000673.2:g.32400023G>T	GRCh38
NC_000011.9:g.32421569G>T , CM000673.1:g.32421569G>T	GRCh37
NC_000011.8:g.32378145G>T	NCBI36
NG_009272.1:g.40519C>A , LRG_525:g.40519C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024426.6:c.1038C>A MANE Select	NP_077744.4:p.Ser346Arg
ENST00000452863.10:c.1038C>A MANE Select	ENSP00000415516.5:p.Ser346Arg
NM_000378.4:c.972C>A	NP_000369.3:p.Ser324Arg
NM_000378.5:c.987C>A	NP_000369.4:p.Ser329Arg
NM_000378.6:c.987C>A	NP_000369.4:p.Ser329Arg
NM_001198551.1:c.387C>A , LRG_525t2:c.387C>A	NP_001185480.1:p.Ser129Arg
NM_001198552.1:c.336C>A	NP_001185481.1:p.Ser112Arg
NM_001198552.2:c.336C>A	NP_001185481.1:p.Ser112Arg
NM_001367854.1:c.-151C>A	NP_001354783.1:n.-151C>A
NM_024424.3:c.1023C>A	NP_077742.2:p.Ser341Arg
NM_024424.4:c.1038C>A	NP_077742.3:p.Ser346Arg
NM_024424.5:c.1038C>A	NP_077742.3:p.Ser346Arg
NM_024426.4:c.1023C>A	NP_077744.3:p.Ser341Arg
NM_024426.5:c.1038C>A	NP_077744.4:p.Ser346Arg
NR_160306.1:n.1370C>A
ENST00000332351.7:c.1023C>A	ENSP00000331327.3:p.Ser341Arg
ENST00000332351.9:c.987C>A	ENSP00000331327.5:p.Ser329Arg
ENST00000379077.7:c.*222C>A	ENSP00000368368.3:n.*222C>A
ENST00000379077.9:c.*222C>A	ENSP00000368368.5:n.*222C>A
ENST00000379079.6:c.387C>A	ENSP00000368370.2:p.Ser129Arg
ENST00000379079.8:c.387C>A	ENSP00000368370.2:p.Ser129Arg
ENST00000448076.7:c.1023C>A	ENSP00000413452.3:p.Ser341Arg
ENST00000448076.9:c.1038C>A	ENSP00000413452.5:p.Ser346Arg
ENST00000452863.7:c.972C>A	ENSP00000415516.3:p.Ser324Arg
ENST00000526685.1:c.-151C>A	ENSP00000436292.1:n.-151C>A
ENST00000526685.2:n.492C>A
ENST00000527775.1:c.276C>A	ENSP00000435351.1:p.Ser92Arg
ENST00000527882.5:c.94C>A
ENST00000530998.5:c.336C>A	ENSP00000435307.1:p.Ser112Arg
ENST00000639563.3:c.987C>A	ENSP00000492269.3:p.Ser329Arg
ENST00000639907.2:n.181C>A
ENST00000640146.2:c.363C>A	ENSP00000491984.2:p.Ser121Arg
ENST00000651794.1:n.781C>A
ENST00000652579.1:n.198C>A
ENST00000652724.1:n.228C>A