Canonical Allele Identifier: CA064579

Gene: WT1

Linked Data

• dbSNP Id: rs745787835
• ExAC: 11:32413470 T / C
• gnomAD v2: 11-32413470-T-C
• gnomAD v3: 11-32391924-T-C
• gnomAD v4: 11-32391924-T-C
• MyVariant Identifiers: chr11:g.32413470T>C (hg19) ; chr11:g.32391924T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391924T>C , CM000673.2:g.32391924T>C	GRCh38
NC_000011.9:g.32413470T>C , CM000673.1:g.32413470T>C	GRCh37
NC_000011.8:g.32370046T>C	NCBI36
NG_009272.1:g.48618A>G , LRG_525:g.48618A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1387+57A>G	ENSP00000331327.5:n.1387+57A>G
ENST00000379077.9:c.*631+48A>G	ENSP00000368368.5:n.*631+48A>G
ENST00000379079.8:c.787+57A>G	ENSP00000368370.2:n.787+57A>G
ENST00000448076.9:c.1438+57A>G	ENSP00000413452.5:n.1438+57A>G
ENST00000452863.10:c.1447+48A>G MANE Select	ENSP00000415516.5:n.1447+48A>G
ENST00000526685.2:n.892+57A>G
ENST00000639563.3:c.1396+48A>G	ENSP00000492269.3:n.1396+48A>G
ENST00000639907.2:n.581+57A>G
ENST00000640146.2:c.772+48A>G	ENSP00000491984.2:n.772+48A>G
ENST00000650745.1:n.1257+48A>G
ENST00000650861.1:n.2019+57A>G
ENST00000650986.1:n.110+48A>G
ENST00000651459.1:c.218+48A>G
ENST00000651533.1:n.484+57A>G
ENST00000651668.1:n.384+48A>G
ENST00000651794.1:n.1290+48A>G
ENST00000651819.1:n.372+48A>G
ENST00000652579.1:n.707+48A>G
ENST00000652724.1:n.637+48A>G
ENST00000332351.7:c.1432+48A>G	ENSP00000331327.3:n.1432+48A>G
ENST00000379077.7:c.*631+48A>G	ENSP00000368368.3:n.*631+48A>G
ENST00000379079.6:c.787+57A>G	ENSP00000368370.2:n.787+57A>G
ENST00000448076.7:c.1423+57A>G	ENSP00000413452.3:n.1423+57A>G
ENST00000452863.7:c.1372+57A>G	ENSP00000415516.3:n.1372+57A>G
ENST00000527882.5:c.413+48A>G
ENST00000530998.5:c.745+48A>G	ENSP00000435307.1:n.745+48A>G
NM_000378.4:c.1372+57A>G	NP_000369.3:n.1372+57A>G
NM_001198551.1:c.787+57A>G , LRG_525t2:c.787+57A>G	NP_001185480.1:n.787+57A>G
NM_001198552.1:c.745+48A>G	NP_001185481.1:n.745+48A>G
NM_024424.3:c.1423+57A>G	NP_077742.2:n.1423+57A>G
NM_024426.4:c.1432+48A>G	NP_077744.3:n.1432+48A>G
NM_000378.5:c.1387+57A>G	NP_000369.4:n.1387+57A>G
NM_024424.4:c.1438+57A>G	NP_077742.3:n.1438+57A>G
NM_024426.5:c.1447+48A>G	NP_077744.4:n.1447+48A>G
NM_001367854.1:c.259+48A>G	NP_001354783.1:n.259+48A>G
NR_160306.1:n.1779+48A>G
NM_000378.6:c.1387+57A>G	NP_000369.4:n.1387+57A>G
NM_001198552.2:c.745+48A>G	NP_001185481.1:n.745+48A>G
NM_024424.5:c.1438+57A>G	NP_077742.3:n.1438+57A>G
NM_024426.6:c.1447+48A>G MANE Select	NP_077744.4:n.1447+48A>G