Canonical Allele Identifier: CA1962327419
Gene: WT1 HGNC NCBI

Linked Data

dbSNP Id: rs1853477065

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32435242_32435251del , CM000673.2:g.32435242_32435251del GRCh38
NC_000011.9:g.32456788_32456797del , CM000673.1:g.32456788_32456797del GRCh37
NC_000011.8:g.32413364_32413373del NCBI36
NG_009272.1:g.5291_5300del , LRG_525:g.5291_5300del

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.110_119del ENSP00000331327.5:p.Gly37AlafsTer9
ENST00000379077.9:c.110_119del ENSP00000368368.5:p.Gly37AlafsTer9
ENST00000448076.9:c.110_119del ENSP00000413452.5:p.Gly37AlafsTer9
ENST00000452863.10:c.110_119del MANE Select ENSP00000415516.5:p.Gly37AlafsTer9
ENST00000639563.3:c.110_119del ENSP00000492269.3:p.Gly37AlafsTer9
ENST00000332351.7:c.95_104del ENSP00000331327.3:p.Gly32AlafsTer9
ENST00000379077.7:c.95_104del ENSP00000368368.3:p.Gly32AlafsTer9
ENST00000448076.7:c.95_104del ENSP00000413452.3:p.Gly32AlafsTer9
ENST00000452863.7:c.95_104del ENSP00000415516.3:p.Gly32AlafsTer9
NM_000378.4:c.95_104del NP_000369.3:p.Gly32AlafsTer9
NM_024424.3:c.95_104del NP_077742.2:p.Gly32AlafsTer9
NM_024426.4:c.95_104del NP_077744.3:p.Gly32AlafsTer9
NM_000378.5:c.110_119del NP_000369.4:p.Gly37AlafsTer9
NM_024424.4:c.110_119del NP_077742.3:p.Gly37AlafsTer9
NM_024426.5:c.110_119del NP_077744.4:p.Gly37AlafsTer9
NR_160306.1:n.289_298del
NM_000378.6:c.110_119del NP_000369.4:p.Gly37AlafsTer9
NM_024424.5:c.110_119del NP_077742.3:p.Gly37AlafsTer9
NM_024426.6:c.110_119del MANE Select NP_077744.4:p.Gly37AlafsTer9