Canonical Allele Identifier: CA1962340420

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32399969G= , CM000673.2:g.32399969G=	GRCh38
NC_000011.9:g.32421515G= , CM000673.1:g.32421515G=	GRCh37
NC_000011.8:g.32378091G=	NCBI36
NG_009272.1:g.40573C= , LRG_525:g.40573C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1041C=	ENSP00000331327.5:p.His347=
ENST00000379077.9:c.*276C=	ENSP00000368368.5:n.*276C=
ENST00000379079.8:c.441C=	ENSP00000368370.2:p.His147=
ENST00000448076.9:c.1092C=	ENSP00000413452.5:p.His364=
ENST00000452863.10:c.1092C= MANE Select	ENSP00000415516.5:p.His364=
ENST00000526685.2:n.546C=
ENST00000639563.3:c.1041C=	ENSP00000492269.3:p.His347=
ENST00000639907.2:n.235C=
ENST00000640146.2:c.417C=	ENSP00000491984.2:p.His139=
ENST00000651459.1:c.14C=
ENST00000651794.1:n.835C=
ENST00000652579.1:n.252C=
ENST00000652724.1:n.282C=
ENST00000332351.7:c.1077C=	ENSP00000331327.3:p.His359=
ENST00000379077.7:c.*276C=	ENSP00000368368.3:n.*276C=
ENST00000379079.6:c.441C=	ENSP00000368370.2:p.His147=
ENST00000448076.7:c.1077C=	ENSP00000413452.3:p.His359=
ENST00000452863.7:c.1026C=	ENSP00000415516.3:p.His342=
ENST00000526685.1:c.-97C=	ENSP00000436292.1:n.-97C=
ENST00000527775.1:c.330C=	ENSP00000435351.1:p.His110=
ENST00000527882.5:c.148C=
ENST00000530998.5:c.390C=	ENSP00000435307.1:p.His130=
NM_000378.4:c.1026C=	NP_000369.3:p.His342=
NM_001198551.1:c.441C= , LRG_525t2:c.441C=	NP_001185480.1:p.His147=
NM_001198552.1:c.390C=	NP_001185481.1:p.His130=
NM_024424.3:c.1077C=	NP_077742.2:p.His359=
NM_024426.4:c.1077C=	NP_077744.3:p.His359=
NM_000378.5:c.1041C=	NP_000369.4:p.His347=
NM_024424.4:c.1092C=	NP_077742.3:p.His364=
NM_024426.5:c.1092C=	NP_077744.4:p.His364=
NM_001367854.1:c.-97C=	NP_001354783.1:n.-97C=
NR_160306.1:n.1424C=
NM_000378.6:c.1041C=	NP_000369.4:p.His347=
NM_001198552.2:c.390C=	NP_001185481.1:p.His130=
NM_024424.5:c.1092C=	NP_077742.3:p.His364=
NM_024426.6:c.1092C= MANE Select	NP_077744.4:p.His364=