Canonical Allele Identifier: CA473568278

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32416528C>T , CM000673.2:g.32416528C>T	GRCh38
NC_000011.9:g.32438074C>T , CM000673.1:g.32438074C>T	GRCh37
NC_000011.8:g.32394650C>T	NCBI36
NG_009272.1:g.24014G>A , LRG_525:g.24014G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024426.6:c.978G>A MANE Select	NP_077744.4:p.Gly326=
ENST00000452863.10:c.978G>A MANE Select	ENSP00000415516.5:p.Gly326=
NM_000378.4:c.950+1049G>A	NP_000369.3:n.950+1049G>A
NM_000378.5:c.965+1049G>A	NP_000369.4:n.965+1049G>A
NM_000378.6:c.965+1049G>A	NP_000369.4:n.965+1049G>A
NM_001198551.1:c.327G>A , LRG_525t2:c.327G>A	NP_001185480.1:p.Gly109=
NM_001198552.1:c.314+1049G>A	NP_001185481.1:n.314+1049G>A
NM_001198552.2:c.314+1049G>A	NP_001185481.1:n.314+1049G>A
NM_024424.3:c.963G>A	NP_077742.2:p.Gly321=
NM_024424.4:c.978G>A	NP_077742.3:p.Gly326=
NM_024424.5:c.978G>A	NP_077742.3:p.Gly326=
NM_024426.4:c.963G>A	NP_077744.3:p.Gly321=
NM_024426.5:c.978G>A	NP_077744.4:p.Gly326=
NR_160306.1:n.1310G>A
ENST00000332351.7:c.963G>A	ENSP00000331327.3:p.Gly321=
ENST00000332351.9:c.965+1049G>A	ENSP00000331327.5:n.965+1049G>A
ENST00000379077.7:c.*162G>A	ENSP00000368368.3:n.*162G>A
ENST00000379077.9:c.*162G>A	ENSP00000368368.5:n.*162G>A
ENST00000379079.6:c.327G>A	ENSP00000368370.2:p.Gly109=
ENST00000379079.8:c.327G>A	ENSP00000368370.2:p.Gly109=
ENST00000448076.7:c.963G>A	ENSP00000413452.3:p.Gly321=
ENST00000448076.9:c.978G>A	ENSP00000413452.5:p.Gly326=
ENST00000452863.7:c.950+1049G>A	ENSP00000415516.3:n.950+1049G>A
ENST00000527775.1:c.216G>A	ENSP00000435351.1:p.Gly72=
ENST00000527882.5:c.34G>A
ENST00000530998.5:c.314+1049G>A	ENSP00000435307.1:n.314+1049G>A
ENST00000639563.3:c.965+1049G>A	ENSP00000492269.3:n.965+1049G>A
ENST00000640146.2:c.341+1049G>A	ENSP00000491984.2:n.341+1049G>A
ENST00000651794.1:n.721G>A