Canonical Allele Identifier: CA1962333899

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32388791C= , CM000673.2:g.32388791C=	GRCh38
NC_000011.9:g.32410337C= , CM000673.1:g.32410337C=	GRCh37
NC_000011.8:g.32366913C=	NCBI36
NG_009272.1:g.51751G= , LRG_525:g.51751G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.*267G=	ENSP00000331327.5:n.*267G=
ENST00000379077.9:c.*1020G=	ENSP00000368368.5:n.*1020G=
ENST00000379079.8:c.*267G=	ENSP00000368370.2:n.*267G=
ENST00000448076.9:c.*267G=	ENSP00000413452.5:n.*267G=
ENST00000452863.10:c.*267G= MANE Select	ENSP00000415516.5:n.*267G=
ENST00000639907.2:n.970G=
ENST00000640146.2:c.*267G=	ENSP00000491984.2:n.*267G=
ENST00000650745.1:n.1646G=
ENST00000650861.1:n.2408G=
ENST00000651459.1:c.607G=
ENST00000651533.1:n.873G=
ENST00000651668.1:n.773G=
ENST00000651794.1:n.1679G=
ENST00000651819.1:n.761G=
ENST00000652579.1:n.1096G=
ENST00000652724.1:n.1026G=
ENST00000332351.7:c.*267G=	ENSP00000331327.3:n.*267G=
ENST00000379077.7:c.*1020G=	ENSP00000368368.3:n.*1020G=
ENST00000379079.6:c.*267G=	ENSP00000368370.2:n.*267G=
ENST00000448076.7:c.*267G=	ENSP00000413452.3:n.*267G=
ENST00000452863.7:c.1761G=	ENSP00000415516.3:n.1761G=
ENST00000530998.5:c.*267G=	ENSP00000435307.1:n.*267G=
NM_000378.4:c.*267G=	NP_000369.3:n.*267G=
NM_001198551.1:c.*267G= , LRG_525t2:c.*267G=	NP_001185480.1:n.*267G=
NM_001198552.1:c.*267G=	NP_001185481.1:n.*267G=
NM_024424.3:c.*267G=	NP_077742.2:n.*267G=
NM_024426.4:c.*267G=	NP_077744.3:n.*267G=
NM_000378.5:c.*267G=	NP_000369.4:n.*267G=
NM_024424.4:c.*267G=	NP_077742.3:n.*267G=
NM_024426.5:c.*267G=	NP_077744.4:n.*267G=
NM_001367854.1:c.*267G=	NP_001354783.1:n.*267G=
NR_160306.1:n.2168G=
NM_000378.6:c.*267G=	NP_000369.4:n.*267G=
NM_001198552.2:c.*267G=	NP_001185481.1:n.*267G=
NM_024424.5:c.*267G=	NP_077742.3:n.*267G=
NM_024426.6:c.*267G= MANE Select	NP_077744.4:n.*267G=