Canonical Allele Identifier: CA1962333966

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32388970T= , CM000673.2:g.32388970T=	GRCh38
NC_000011.9:g.32410516T= , CM000673.1:g.32410516T=	GRCh37
NC_000011.8:g.32367092T=	NCBI36
NG_009272.1:g.51572A= , LRG_525:g.51572A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.*88A=	ENSP00000331327.5:n.*88A=
ENST00000379077.9:c.*841A=	ENSP00000368368.5:n.*841A=
ENST00000379079.8:c.*88A=	ENSP00000368370.2:n.*88A=
ENST00000448076.9:c.*88A=	ENSP00000413452.5:n.*88A=
ENST00000452863.10:c.*88A= MANE Select	ENSP00000415516.5:n.*88A=
ENST00000639907.2:n.791A=
ENST00000640146.2:c.*88A=	ENSP00000491984.2:n.*88A=
ENST00000650745.1:n.1467A=
ENST00000650861.1:n.2229A=
ENST00000651459.1:c.428A=
ENST00000651533.1:n.694A=
ENST00000651668.1:n.594A=
ENST00000651794.1:n.1500A=
ENST00000651819.1:n.582A=
ENST00000652579.1:n.917A=
ENST00000652724.1:n.847A=
ENST00000332351.7:c.*88A=	ENSP00000331327.3:n.*88A=
ENST00000379077.7:c.*841A=	ENSP00000368368.3:n.*841A=
ENST00000379079.6:c.*88A=	ENSP00000368370.2:n.*88A=
ENST00000448076.7:c.*88A=	ENSP00000413452.3:n.*88A=
ENST00000452863.7:c.1582A=	ENSP00000415516.3:n.1582A=
ENST00000530998.5:c.*88A=	ENSP00000435307.1:n.*88A=
NM_000378.4:c.*88A=	NP_000369.3:n.*88A=
NM_001198551.1:c.*88A= , LRG_525t2:c.*88A=	NP_001185480.1:n.*88A=
NM_001198552.1:c.*88A=	NP_001185481.1:n.*88A=
NM_024424.3:c.*88A=	NP_077742.2:n.*88A=
NM_024426.4:c.*88A=	NP_077744.3:n.*88A=
NM_000378.5:c.*88A=	NP_000369.4:n.*88A=
NM_024424.4:c.*88A=	NP_077742.3:n.*88A=
NM_024426.5:c.*88A=	NP_077744.4:n.*88A=
NM_001367854.1:c.*88A=	NP_001354783.1:n.*88A=
NR_160306.1:n.1989A=
NM_000378.6:c.*88A=	NP_000369.4:n.*88A=
NM_001198552.2:c.*88A=	NP_001185481.1:n.*88A=
NM_024424.5:c.*88A=	NP_077742.3:n.*88A=
NM_024426.6:c.*88A= MANE Select	NP_077744.4:n.*88A=