Canonical Allele Identifier: CA1962335546

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392689T= , CM000673.2:g.32392689T=	GRCh38
NC_000011.9:g.32414235T= , CM000673.1:g.32414235T=	GRCh37
NC_000011.8:g.32370811T=	NCBI36
NG_009272.1:g.47853A= , LRG_525:g.47853A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1280A=	ENSP00000331327.5:p.Lys427=
ENST00000379077.9:c.*515A=	ENSP00000368368.5:n.*515A=
ENST00000379079.8:c.680A=	ENSP00000368370.2:p.Lys227=
ENST00000448076.9:c.1331A=	ENSP00000413452.5:p.Lys444=
ENST00000452863.10:c.1331A= MANE Select	ENSP00000415516.5:p.Lys444=
ENST00000526685.2:n.785A=
ENST00000639563.3:c.1280A=	ENSP00000492269.3:p.Lys427=
ENST00000639907.2:n.474A=
ENST00000640146.2:c.656A=	ENSP00000491984.2:p.Lys219=
ENST00000650745.1:n.540A=
ENST00000650861.1:n.1912A=
ENST00000651459.1:c.102A=
ENST00000651533.1:n.377A=
ENST00000651668.1:n.268A=
ENST00000651794.1:n.1174A=
ENST00000651819.1:n.256A=
ENST00000652579.1:n.591A=
ENST00000652724.1:n.521A=
ENST00000332351.7:c.1316A=	ENSP00000331327.3:p.Lys439=
ENST00000379077.7:c.*515A=	ENSP00000368368.3:n.*515A=
ENST00000379079.6:c.680A=	ENSP00000368370.2:p.Lys227=
ENST00000448076.7:c.1316A=	ENSP00000413452.3:p.Lys439=
ENST00000452863.7:c.1265A=	ENSP00000415516.3:p.Lys422=
ENST00000527882.5:c.321-625A=
ENST00000530998.5:c.629A=	ENSP00000435307.1:p.Lys210=
NM_000378.4:c.1265A=	NP_000369.3:p.Lys422=
NM_001198551.1:c.680A= , LRG_525t2:c.680A=	NP_001185480.1:p.Lys227=
NM_001198552.1:c.629A=	NP_001185481.1:p.Lys210=
NM_024424.3:c.1316A=	NP_077742.2:p.Lys439=
NM_024426.4:c.1316A=	NP_077744.3:p.Lys439=
NM_000378.5:c.1280A=	NP_000369.4:p.Lys427=
NM_024424.4:c.1331A=	NP_077742.3:p.Lys444=
NM_024426.5:c.1331A=	NP_077744.4:p.Lys444=
NM_001367854.1:c.143A=	NP_001354783.1:p.Lys48=
NR_160306.1:n.1663A=
NM_000378.6:c.1280A=	NP_000369.4:p.Lys427=
NM_001198552.2:c.629A=	NP_001185481.1:p.Lys210=
NM_024424.5:c.1331A=	NP_077742.3:p.Lys444=
NM_024426.6:c.1331A= MANE Select	NP_077744.4:p.Lys444=