Canonical Allele Identifier: CA1962326998
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32434567C= , CM000673.2:g.32434567C= GRCh38
NC_000011.9:g.32456113C= , CM000673.1:g.32456113C= GRCh37
NC_000011.8:g.32412689C= NCBI36
NG_009272.1:g.5975G= , LRG_525:g.5975G=

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.661+133G= ENSP00000331327.5:n.661+133G=
ENST00000379077.9:c.661+133G= ENSP00000368368.5:n.661+133G=
ENST00000448076.9:c.661+133G= ENSP00000413452.5:n.661+133G=
ENST00000452863.10:c.661+133G= MANE Select ENSP00000415516.5:n.661+133G=
ENST00000639563.3:c.661+133G= ENSP00000492269.3:n.661+133G=
ENST00000332351.7:c.646+133G= ENSP00000331327.3:n.646+133G=
ENST00000379077.7:c.646+133G= ENSP00000368368.3:n.646+133G=
ENST00000448076.7:c.646+133G= ENSP00000413452.3:n.646+133G=
ENST00000452863.7:c.646+133G= ENSP00000415516.3:n.646+133G=
NM_000378.4:c.646+133G= NP_000369.3:n.646+133G=
NM_024424.3:c.646+133G= NP_077742.2:n.646+133G=
NM_024426.4:c.646+133G= NP_077744.3:n.646+133G=
NM_000378.5:c.661+133G= NP_000369.4:n.661+133G=
NM_024424.4:c.661+133G= NP_077742.3:n.661+133G=
NM_024426.5:c.661+133G= NP_077744.4:n.661+133G=
NR_160306.1:n.840+133G=
NM_000378.6:c.661+133G= NP_000369.4:n.661+133G=
NM_024424.5:c.661+133G= NP_077742.3:n.661+133G=
NM_024426.6:c.661+133G= MANE Select NP_077744.4:n.661+133G=