Canonical Allele Identifier: CA1962335247

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391981C= , CM000673.2:g.32391981C=	GRCh38
NC_000011.9:g.32413527C= , CM000673.1:g.32413527C=	GRCh37
NC_000011.8:g.32370103C=	NCBI36
NG_009272.1:g.48561G= , LRG_525:g.48561G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1387G=	ENSP00000331327.5:p.Gly463=
ENST00000379077.9:c.*622G=	ENSP00000368368.5:n.*622G=
ENST00000379079.8:c.787G=	ENSP00000368370.2:p.Gly263=
ENST00000448076.9:c.1438G=	ENSP00000413452.5:p.Gly480=
ENST00000452863.10:c.1438G= MANE Select	ENSP00000415516.5:p.Gly480=
ENST00000526685.2:n.892G=
ENST00000639563.3:c.1387G=	ENSP00000492269.3:p.Gly463=
ENST00000639907.2:n.581G=
ENST00000640146.2:c.763G=	ENSP00000491984.2:p.Gly255=
ENST00000650745.1:n.1248G=
ENST00000650861.1:n.2019G=
ENST00000650986.1:n.101G=
ENST00000651459.1:c.209G=
ENST00000651533.1:n.484G=
ENST00000651668.1:n.375G=
ENST00000651794.1:n.1281G=
ENST00000651819.1:n.363G=
ENST00000652579.1:n.698G=
ENST00000652724.1:n.628G=
ENST00000332351.7:c.1423G=	ENSP00000331327.3:p.Gly475=
ENST00000379077.7:c.*622G=	ENSP00000368368.3:n.*622G=
ENST00000379079.6:c.787G=	ENSP00000368370.2:p.Gly263=
ENST00000448076.7:c.1423G=	ENSP00000413452.3:p.Gly475=
ENST00000452863.7:c.1372G=	ENSP00000415516.3:p.Gly458=
ENST00000527882.5:c.404G=
ENST00000530998.5:c.736G=	ENSP00000435307.1:p.Gly246=
NM_000378.4:c.1372G=	NP_000369.3:p.Gly458=
NM_001198551.1:c.787G= , LRG_525t2:c.787G=	NP_001185480.1:p.Gly263=
NM_001198552.1:c.736G=	NP_001185481.1:p.Gly246=
NM_024424.3:c.1423G=	NP_077742.2:p.Gly475=
NM_024426.4:c.1423G=	NP_077744.3:p.Gly475=
NM_000378.5:c.1387G=	NP_000369.4:p.Gly463=
NM_024424.4:c.1438G=	NP_077742.3:p.Gly480=
NM_024426.5:c.1438G=	NP_077744.4:p.Gly480=
NM_001367854.1:c.250G=	NP_001354783.1:p.Gly84=
NR_160306.1:n.1770G=
NM_000378.6:c.1387G=	NP_000369.4:p.Gly463=
NM_001198552.2:c.736G=	NP_001185481.1:p.Gly246=
NM_024424.5:c.1438G=	NP_077742.3:p.Gly480=
NM_024426.6:c.1438G= MANE Select	NP_077744.4:p.Gly480=