Canonical Allele Identifier: CA379959411
Gene: WT1 HGNC NCBI

Linked Data

dbSNP Id: rs2132921399

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392741G>A , CM000673.2:g.32392741G>A GRCh38
NC_000011.9:g.32414287G>A , CM000673.1:g.32414287G>A GRCh37
NC_000011.8:g.32370863G>A NCBI36
NG_009272.1:g.47801C>T , LRG_525:g.47801C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1228C>T ENSP00000331327.5:p.Gln410Ter
ENST00000379077.9:c.*463C>T ENSP00000368368.5:n.*463C>T
ENST00000379079.8:c.628C>T ENSP00000368370.2:p.Gln210Ter
ENST00000448076.9:c.1279C>T ENSP00000413452.5:p.Gln427Ter
ENST00000452863.10:c.1279C>T MANE Select ENSP00000415516.5:p.Gln427Ter
ENST00000526685.2:n.733C>T
ENST00000639563.3:c.1228C>T ENSP00000492269.3:p.Gln410Ter
ENST00000639907.2:n.422C>T
ENST00000640146.2:c.604C>T ENSP00000491984.2:p.Gln202Ter
ENST00000650745.1:n.488C>T
ENST00000650861.1:n.1860C>T
ENST00000651459.1:c.50C>T
ENST00000651533.1:n.325C>T
ENST00000651668.1:n.216C>T
ENST00000651794.1:n.1122C>T
ENST00000651819.1:n.204C>T
ENST00000652579.1:n.539C>T
ENST00000652724.1:n.469C>T
ENST00000332351.7:c.1264C>T ENSP00000331327.3:p.Gln422Ter
ENST00000379077.7:c.*463C>T ENSP00000368368.3:n.*463C>T
ENST00000379079.6:c.628C>T ENSP00000368370.2:p.Gln210Ter
ENST00000448076.7:c.1264C>T ENSP00000413452.3:p.Gln422Ter
ENST00000452863.7:c.1213C>T ENSP00000415516.3:p.Gln405Ter
ENST00000527882.5:c.321-677C>T
ENST00000530998.5:c.577C>T ENSP00000435307.1:p.Gln193Ter
NM_000378.4:c.1213C>T NP_000369.3:p.Gln405Ter
NM_001198551.1:c.628C>T , LRG_525t2:c.628C>T NP_001185480.1:p.Gln210Ter
NM_001198552.1:c.577C>T NP_001185481.1:p.Gln193Ter
NM_024424.3:c.1264C>T NP_077742.2:p.Gln422Ter
NM_024426.4:c.1264C>T NP_077744.3:p.Gln422Ter
NM_000378.5:c.1228C>T NP_000369.4:p.Gln410Ter
NM_024424.4:c.1279C>T NP_077742.3:p.Gln427Ter
NM_024426.5:c.1279C>T NP_077744.4:p.Gln427Ter
NM_001367854.1:c.91C>T NP_001354783.1:p.Gln31Ter
NR_160306.1:n.1611C>T
NM_000378.6:c.1228C>T NP_000369.4:p.Gln410Ter
NM_001198552.2:c.577C>T NP_001185481.1:p.Gln193Ter
NM_024424.5:c.1279C>T NP_077742.3:p.Gln427Ter
NM_024426.6:c.1279C>T MANE Select NP_077744.4:p.Gln427Ter