Canonical Allele Identifier: CA1962335545

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392688T= , CM000673.2:g.32392688T=	GRCh38
NC_000011.9:g.32414234T= , CM000673.1:g.32414234T=	GRCh37
NC_000011.8:g.32370810T=	NCBI36
NG_009272.1:g.47854A= , LRG_525:g.47854A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1281A=	ENSP00000331327.5:p.Lys427=
ENST00000379077.9:c.*516A=	ENSP00000368368.5:n.*516A=
ENST00000379079.8:c.681A=	ENSP00000368370.2:p.Lys227=
ENST00000448076.9:c.1332A=	ENSP00000413452.5:p.Lys444=
ENST00000452863.10:c.1332A= MANE Select	ENSP00000415516.5:p.Lys444=
ENST00000526685.2:n.786A=
ENST00000639563.3:c.1281A=	ENSP00000492269.3:p.Lys427=
ENST00000639907.2:n.475A=
ENST00000640146.2:c.657A=	ENSP00000491984.2:p.Lys219=
ENST00000650745.1:n.541A=
ENST00000650861.1:n.1913A=
ENST00000651459.1:c.103A=
ENST00000651533.1:n.378A=
ENST00000651668.1:n.269A=
ENST00000651794.1:n.1175A=
ENST00000651819.1:n.257A=
ENST00000652579.1:n.592A=
ENST00000652724.1:n.522A=
ENST00000332351.7:c.1317A=	ENSP00000331327.3:p.Lys439=
ENST00000379077.7:c.*516A=	ENSP00000368368.3:n.*516A=
ENST00000379079.6:c.681A=	ENSP00000368370.2:p.Lys227=
ENST00000448076.7:c.1317A=	ENSP00000413452.3:p.Lys439=
ENST00000452863.7:c.1266A=	ENSP00000415516.3:p.Lys422=
ENST00000527882.5:c.321-624A=
ENST00000530998.5:c.630A=	ENSP00000435307.1:p.Lys210=
NM_000378.4:c.1266A=	NP_000369.3:p.Lys422=
NM_001198551.1:c.681A= , LRG_525t2:c.681A=	NP_001185480.1:p.Lys227=
NM_001198552.1:c.630A=	NP_001185481.1:p.Lys210=
NM_024424.3:c.1317A=	NP_077742.2:p.Lys439=
NM_024426.4:c.1317A=	NP_077744.3:p.Lys439=
NM_000378.5:c.1281A=	NP_000369.4:p.Lys427=
NM_024424.4:c.1332A=	NP_077742.3:p.Lys444=
NM_024426.5:c.1332A=	NP_077744.4:p.Lys444=
NM_001367854.1:c.144A=	NP_001354783.1:p.Lys48=
NR_160306.1:n.1664A=
NM_000378.6:c.1281A=	NP_000369.4:p.Lys427=
NM_001198552.2:c.630A=	NP_001185481.1:p.Lys210=
NM_024424.5:c.1332A=	NP_077742.3:p.Lys444=
NM_024426.6:c.1332A= MANE Select	NP_077744.4:p.Lys444=