Canonical Allele Identifier: CA473565395

Gene: WT1

Linked Data

• ClinVar Variation Id: 1107591
• ClinVar RCV Id: RCV001432758
• dbSNP Id: rs1851833175
• gnomAD v4: 11-32392030-T-C
• MyVariant Identifiers: chr11:g.32413576T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392030T>C , CM000673.2:g.32392030T>C	GRCh38
NC_000011.9:g.32413576T>C , CM000673.1:g.32413576T>C	GRCh37
NC_000011.8:g.32370152T>C	NCBI36
NG_009272.1:g.48512A>G , LRG_525:g.48512A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1338A>G	ENSP00000331327.5:p.Arg446=
ENST00000379077.9:c.*573A>G	ENSP00000368368.5:n.*573A>G
ENST00000379079.8:c.738A>G	ENSP00000368370.2:p.Arg246=
ENST00000448076.9:c.1389A>G	ENSP00000413452.5:p.Arg463=
ENST00000452863.10:c.1389A>G MANE Select	ENSP00000415516.5:p.Arg463=
ENST00000526685.2:n.843A>G
ENST00000639563.3:c.1338A>G	ENSP00000492269.3:p.Arg446=
ENST00000639907.2:n.532A>G
ENST00000640146.2:c.714A>G	ENSP00000491984.2:p.Arg238=
ENST00000650745.1:n.1199A>G
ENST00000650861.1:n.1970A>G
ENST00000650986.1:n.52A>G
ENST00000651459.1:c.160A>G
ENST00000651533.1:n.435A>G
ENST00000651668.1:n.326A>G
ENST00000651794.1:n.1232A>G
ENST00000651819.1:n.314A>G
ENST00000652579.1:n.649A>G
ENST00000652724.1:n.579A>G
ENST00000332351.7:c.1374A>G	ENSP00000331327.3:p.Arg458=
ENST00000379077.7:c.*573A>G	ENSP00000368368.3:n.*573A>G
ENST00000379079.6:c.738A>G	ENSP00000368370.2:p.Arg246=
ENST00000448076.7:c.1374A>G	ENSP00000413452.3:p.Arg458=
ENST00000452863.7:c.1323A>G	ENSP00000415516.3:p.Arg441=
ENST00000527882.5:c.355A>G
ENST00000530998.5:c.687A>G	ENSP00000435307.1:p.Arg229=
NM_000378.4:c.1323A>G	NP_000369.3:p.Arg441=
NM_001198551.1:c.738A>G , LRG_525t2:c.738A>G	NP_001185480.1:p.Arg246=
NM_001198552.1:c.687A>G	NP_001185481.1:p.Arg229=
NM_024424.3:c.1374A>G	NP_077742.2:p.Arg458=
NM_024426.4:c.1374A>G	NP_077744.3:p.Arg458=
NM_000378.5:c.1338A>G	NP_000369.4:p.Arg446=
NM_024424.4:c.1389A>G	NP_077742.3:p.Arg463=
NM_024426.5:c.1389A>G	NP_077744.4:p.Arg463=
NM_001367854.1:c.201A>G	NP_001354783.1:p.Arg67=
NR_160306.1:n.1721A>G
NM_000378.6:c.1338A>G	NP_000369.4:p.Arg446=
NM_001198552.2:c.687A>G	NP_001185481.1:p.Arg229=
NM_024424.5:c.1389A>G	NP_077742.3:p.Arg463=
NM_024426.6:c.1389A>G MANE Select	NP_077744.4:p.Arg463=