Canonical Allele Identifier: CA379958689
Gene: WT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32391981C>A , CM000673.2:g.32391981C>A GRCh38
NC_000011.9:g.32413527C>A , CM000673.1:g.32413527C>A GRCh37
NC_000011.8:g.32370103C>A NCBI36
NG_009272.1:g.48561G>T , LRG_525:g.48561G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1387G>T ENSP00000331327.5:p.Gly463Cys
ENST00000379077.9:c.*622G>T ENSP00000368368.5:n.*622G>T
ENST00000379079.8:c.787G>T ENSP00000368370.2:p.Gly263Cys
ENST00000448076.9:c.1438G>T ENSP00000413452.5:p.Gly480Cys
ENST00000452863.10:c.1438G>T MANE Select ENSP00000415516.5:p.Gly480Cys
ENST00000526685.2:n.892G>T
ENST00000639563.3:c.1387G>T ENSP00000492269.3:p.Gly463Cys
ENST00000639907.2:n.581G>T
ENST00000640146.2:c.763G>T ENSP00000491984.2:p.Gly255Cys
ENST00000650745.1:n.1248G>T
ENST00000650861.1:n.2019G>T
ENST00000650986.1:n.101G>T
ENST00000651459.1:c.209G>T
ENST00000651533.1:n.484G>T
ENST00000651668.1:n.375G>T
ENST00000651794.1:n.1281G>T
ENST00000651819.1:n.363G>T
ENST00000652579.1:n.698G>T
ENST00000652724.1:n.628G>T
ENST00000332351.7:c.1423G>T ENSP00000331327.3:p.Gly475Cys
ENST00000379077.7:c.*622G>T ENSP00000368368.3:n.*622G>T
ENST00000379079.6:c.787G>T ENSP00000368370.2:p.Gly263Cys
ENST00000448076.7:c.1423G>T ENSP00000413452.3:p.Gly475Cys
ENST00000452863.7:c.1372G>T ENSP00000415516.3:p.Gly458Cys
ENST00000527882.5:c.404G>T
ENST00000530998.5:c.736G>T ENSP00000435307.1:p.Gly246Cys
NM_000378.4:c.1372G>T NP_000369.3:p.Gly458Cys
NM_001198551.1:c.787G>T , LRG_525t2:c.787G>T NP_001185480.1:p.Gly263Cys
NM_001198552.1:c.736G>T NP_001185481.1:p.Gly246Cys
NM_024424.3:c.1423G>T NP_077742.2:p.Gly475Cys
NM_024426.4:c.1423G>T NP_077744.3:p.Gly475Cys
NM_000378.5:c.1387G>T NP_000369.4:p.Gly463Cys
NM_024424.4:c.1438G>T NP_077742.3:p.Gly480Cys
NM_024426.5:c.1438G>T NP_077744.4:p.Gly480Cys
NM_001367854.1:c.250G>T NP_001354783.1:p.Gly84Cys
NR_160306.1:n.1770G>T
NM_000378.6:c.1387G>T NP_000369.4:p.Gly463Cys
NM_001198552.2:c.736G>T NP_001185481.1:p.Gly246Cys
NM_024424.5:c.1438G>T NP_077742.3:p.Gly480Cys
NM_024426.6:c.1438G>T MANE Select NP_077744.4:p.Gly480Cys