Canonical Allele Identifier: CA379958972

Gene: WT1

Linked Data

• gnomAD v4: 11-32392049-T-C
• MyVariant Identifiers: chr11:g.32413595T>C (hg19) ; chr11:g.32392049T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392049T>C , CM000673.2:g.32392049T>C	GRCh38
NC_000011.9:g.32413595T>C , CM000673.1:g.32413595T>C	GRCh37
NC_000011.8:g.32370171T>C	NCBI36
NG_009272.1:g.48493A>G , LRG_525:g.48493A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1319A>G	ENSP00000331327.5:p.Gln440Arg
ENST00000379077.9:c.*554A>G	ENSP00000368368.5:n.*554A>G
ENST00000379079.8:c.719A>G	ENSP00000368370.2:p.Gln240Arg
ENST00000448076.9:c.1370A>G	ENSP00000413452.5:p.Gln457Arg
ENST00000452863.10:c.1370A>G MANE Select	ENSP00000415516.5:p.Gln457Arg
ENST00000526685.2:n.824A>G
ENST00000639563.3:c.1319A>G	ENSP00000492269.3:p.Gln440Arg
ENST00000639907.2:n.513A>G
ENST00000640146.2:c.695A>G	ENSP00000491984.2:p.Gln232Arg
ENST00000650745.1:n.1180A>G
ENST00000650861.1:n.1951A>G
ENST00000650986.1:n.33A>G
ENST00000651459.1:c.141A>G
ENST00000651533.1:n.416A>G
ENST00000651668.1:n.307A>G
ENST00000651794.1:n.1213A>G
ENST00000651819.1:n.295A>G
ENST00000652579.1:n.630A>G
ENST00000652724.1:n.560A>G
ENST00000332351.7:c.1355A>G	ENSP00000331327.3:p.Gln452Arg
ENST00000379077.7:c.*554A>G	ENSP00000368368.3:n.*554A>G
ENST00000379079.6:c.719A>G	ENSP00000368370.2:p.Gln240Arg
ENST00000448076.7:c.1355A>G	ENSP00000413452.3:p.Gln452Arg
ENST00000452863.7:c.1304A>G	ENSP00000415516.3:p.Gln435Arg
ENST00000527882.5:c.336A>G
ENST00000530998.5:c.668A>G	ENSP00000435307.1:p.Gln223Arg
NM_000378.4:c.1304A>G	NP_000369.3:p.Gln435Arg
NM_001198551.1:c.719A>G , LRG_525t2:c.719A>G	NP_001185480.1:p.Gln240Arg
NM_001198552.1:c.668A>G	NP_001185481.1:p.Gln223Arg
NM_024424.3:c.1355A>G	NP_077742.2:p.Gln452Arg
NM_024426.4:c.1355A>G	NP_077744.3:p.Gln452Arg
NM_000378.5:c.1319A>G	NP_000369.4:p.Gln440Arg
NM_024424.4:c.1370A>G	NP_077742.3:p.Gln457Arg
NM_024426.5:c.1370A>G	NP_077744.4:p.Gln457Arg
NM_001367854.1:c.182A>G	NP_001354783.1:p.Gln61Arg
NR_160306.1:n.1702A>G
NM_000378.6:c.1319A>G	NP_000369.4:p.Gln440Arg
NM_001198552.2:c.668A>G	NP_001185481.1:p.Gln223Arg
NM_024424.5:c.1370A>G	NP_077742.3:p.Gln457Arg
NM_024426.6:c.1370A>G MANE Select	NP_077744.4:p.Gln457Arg