Canonical Allele Identifier: CA1962340685

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32400157A= , CM000673.2:g.32400157A=	GRCh38
NC_000011.9:g.32421703A= , CM000673.1:g.32421703A=	GRCh37
NC_000011.8:g.32378279A=	NCBI36
NG_009272.1:g.40385T= , LRG_525:g.40385T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.966-113T=	ENSP00000331327.5:n.966-113T=
ENST00000379077.9:c.*201-113T=	ENSP00000368368.5:n.*201-113T=
ENST00000379079.8:c.366-113T=	ENSP00000368370.2:n.366-113T=
ENST00000448076.9:c.1017-113T=	ENSP00000413452.5:n.1017-113T=
ENST00000452863.10:c.1017-113T= MANE Select	ENSP00000415516.5:n.1017-113T=
ENST00000526685.2:n.459T=
ENST00000639563.3:c.966-113T=	ENSP00000492269.3:n.966-113T=
ENST00000639907.2:n.47T=
ENST00000640146.2:c.342-113T=	ENSP00000491984.2:n.342-113T=
ENST00000651794.1:n.760-113T=
ENST00000652579.1:n.177-113T=
ENST00000652724.1:n.195T=
ENST00000332351.7:c.1002-113T=	ENSP00000331327.3:n.1002-113T=
ENST00000379077.7:c.*201-113T=	ENSP00000368368.3:n.*201-113T=
ENST00000379079.6:c.366-113T=	ENSP00000368370.2:n.366-113T=
ENST00000448076.7:c.1002-113T=	ENSP00000413452.3:n.1002-113T=
ENST00000452863.7:c.951-113T=	ENSP00000415516.3:n.951-113T=
ENST00000526685.1:c.-184T=	ENSP00000436292.1:n.-184T=
ENST00000527775.1:c.255-113T=	ENSP00000435351.1:n.255-113T=
ENST00000527882.5:c.73-113T=
ENST00000530998.5:c.315-113T=	ENSP00000435307.1:n.315-113T=
NM_000378.4:c.951-113T=	NP_000369.3:n.951-113T=
NM_001198551.1:c.366-113T= , LRG_525t2:c.366-113T=	NP_001185480.1:n.366-113T=
NM_001198552.1:c.315-113T=	NP_001185481.1:n.315-113T=
NM_024424.3:c.1002-113T=	NP_077742.2:n.1002-113T=
NM_024426.4:c.1002-113T=	NP_077744.3:n.1002-113T=
NM_000378.5:c.966-113T=	NP_000369.4:n.966-113T=
NM_024424.4:c.1017-113T=	NP_077742.3:n.1017-113T=
NM_024426.5:c.1017-113T=	NP_077744.4:n.1017-113T=
NM_001367854.1:c.-184T=	NP_001354783.1:n.-184T=
NR_160306.1:n.1349-113T=
NM_000378.6:c.966-113T=	NP_000369.4:n.966-113T=
NM_001198552.2:c.315-113T=	NP_001185481.1:n.315-113T=
NM_024424.5:c.1017-113T=	NP_077742.3:n.1017-113T=
NM_024426.6:c.1017-113T= MANE Select	NP_077744.4:n.1017-113T=