Canonical Allele Identifier: CA064462

Gene: WT1

Linked Data

• dbSNP Id: rs769499906
• ExAC: 11:32414220 C / T
• gnomAD v2: 11-32414220-C-T
• MyVariant Identifiers: chr11:g.32414220C>T (hg19) ; chr11:g.32392674C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392674C>T , CM000673.2:g.32392674C>T	GRCh38
NC_000011.9:g.32414220C>T , CM000673.1:g.32414220C>T	GRCh37
NC_000011.8:g.32370796C>T	NCBI36
NG_009272.1:g.47868G>A , LRG_525:g.47868G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1295G>A	ENSP00000331327.5:p.Arg432Lys
ENST00000379077.9:c.*530G>A	ENSP00000368368.5:n.*530G>A
ENST00000379079.8:c.695G>A	ENSP00000368370.2:p.Arg232Lys
ENST00000448076.9:c.1346G>A	ENSP00000413452.5:p.Arg449Lys
ENST00000452863.10:c.1346G>A MANE Select	ENSP00000415516.5:p.Arg449Lys
ENST00000526685.2:n.800G>A
ENST00000639563.3:c.1295G>A	ENSP00000492269.3:p.Arg432Lys
ENST00000639907.2:n.489G>A
ENST00000640146.2:c.671G>A	ENSP00000491984.2:p.Arg224Lys
ENST00000650745.1:n.555G>A
ENST00000650861.1:n.1927G>A
ENST00000651459.1:c.117G>A
ENST00000651533.1:n.392G>A
ENST00000651668.1:n.283G>A
ENST00000651794.1:n.1189G>A
ENST00000651819.1:n.271G>A
ENST00000652579.1:n.606G>A
ENST00000652724.1:n.536G>A
ENST00000332351.7:c.1331G>A	ENSP00000331327.3:p.Arg444Lys
ENST00000379077.7:c.*530G>A	ENSP00000368368.3:n.*530G>A
ENST00000379079.6:c.695G>A	ENSP00000368370.2:p.Arg232Lys
ENST00000448076.7:c.1331G>A	ENSP00000413452.3:p.Arg444Lys
ENST00000452863.7:c.1280G>A	ENSP00000415516.3:p.Arg427Lys
ENST00000527882.5:c.321-610G>A
ENST00000530998.5:c.644G>A	ENSP00000435307.1:p.Arg215Lys
NM_000378.4:c.1280G>A	NP_000369.3:p.Arg427Lys
NM_001198551.1:c.695G>A , LRG_525t2:c.695G>A	NP_001185480.1:p.Arg232Lys
NM_001198552.1:c.644G>A	NP_001185481.1:p.Arg215Lys
NM_024424.3:c.1331G>A	NP_077742.2:p.Arg444Lys
NM_024426.4:c.1331G>A	NP_077744.3:p.Arg444Lys
NM_000378.5:c.1295G>A	NP_000369.4:p.Arg432Lys
NM_024424.4:c.1346G>A	NP_077742.3:p.Arg449Lys
NM_024426.5:c.1346G>A	NP_077744.4:p.Arg449Lys
NM_001367854.1:c.158G>A	NP_001354783.1:p.Arg53Lys
NR_160306.1:n.1678G>A
NM_000378.6:c.1295G>A	NP_000369.4:p.Arg432Lys
NM_001198552.2:c.644G>A	NP_001185481.1:p.Arg215Lys
NM_024424.5:c.1346G>A	NP_077742.3:p.Arg449Lys
NM_024426.6:c.1346G>A MANE Select	NP_077744.4:p.Arg449Lys