Canonical Allele Identifier: CA1962327489

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435365G= , CM000673.2:g.32435365G=	GRCh38
NC_000011.9:g.32456911G= , CM000673.1:g.32456911G=	GRCh37
NC_000011.8:g.32413487G=	NCBI36
NG_009272.1:g.5177C= , LRG_525:g.5177C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.-5C=	ENSP00000331327.5:n.-5C=
ENST00000379077.9:c.-5C=	ENSP00000368368.5:n.-5C=
ENST00000448076.9:c.-5C=	ENSP00000413452.5:n.-5C=
ENST00000452863.10:c.-5C= MANE Select	ENSP00000415516.5:n.-5C=
ENST00000332351.7:c.-20C=	ENSP00000331327.3:n.-20C=
ENST00000379077.7:c.-20C=	ENSP00000368368.3:n.-20C=
ENST00000448076.7:c.-20C=	ENSP00000413452.3:n.-20C=
NM_000378.4:c.-20C=	NP_000369.3:n.-20C=
NM_024424.3:c.-20C=	NP_077742.2:n.-20C=
NM_024426.4:c.-20C=	NP_077744.3:n.-20C=
NM_000378.5:c.-5C=	NP_000369.4:n.-5C=
NM_024424.4:c.-5C=	NP_077742.3:n.-5C=
NM_024426.5:c.-5C=	NP_077744.4:n.-5C=
NR_160306.1:n.175C=
NM_000378.6:c.-5C=	NP_000369.4:n.-5C=
NM_024424.5:c.-5C=	NP_077742.3:n.-5C=
NM_024426.6:c.-5C= MANE Select	NP_077744.4:n.-5C=