Canonical Allele Identifier: CA1962327411
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32435235_32435236delinsGC , CM000673.2:g.32435235_32435236delinsGC GRCh38
NC_000011.9:g.32456781_32456782delinsGC , CM000673.1:g.32456781_32456782delinsGC GRCh37
NC_000011.8:g.32413357_32413358delinsGC NCBI36
NG_009272.1:g.5306_5307delinsGC , LRG_525:g.5306_5307delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.125_126delinsGC ENSP00000331327.5:p.Gly42=
ENST00000379077.9:c.125_126delinsGC ENSP00000368368.5:p.Gly42=
ENST00000448076.9:c.125_126delinsGC ENSP00000413452.5:p.Gly42=
ENST00000452863.10:c.125_126delinsGC MANE Select ENSP00000415516.5:p.Gly42=
ENST00000639563.3:c.125_126delinsGC ENSP00000492269.3:p.Gly42=
ENST00000332351.7:c.110_111delinsGC ENSP00000331327.3:p.Gly37=
ENST00000379077.7:c.110_111delinsGC ENSP00000368368.3:p.Gly37=
ENST00000448076.7:c.110_111delinsGC ENSP00000413452.3:p.Gly37=
ENST00000452863.7:c.110_111delinsGC ENSP00000415516.3:p.Gly37=
NM_000378.4:c.110_111delinsGC NP_000369.3:p.Gly37=
NM_024424.3:c.110_111delinsGC NP_077742.2:p.Gly37=
NM_024426.4:c.110_111delinsGC NP_077744.3:p.Gly37=
NM_000378.5:c.125_126delinsGC NP_000369.4:p.Gly42=
NM_024424.4:c.125_126delinsGC NP_077742.3:p.Gly42=
NM_024426.5:c.125_126delinsGC NP_077744.4:p.Gly42=
NR_160306.1:n.304_305delinsGC
NM_000378.6:c.125_126delinsGC NP_000369.4:p.Gly42=
NM_024424.5:c.125_126delinsGC NP_077742.3:p.Gly42=
NM_024426.6:c.125_126delinsGC MANE Select NP_077744.4:p.Gly42=