Canonical Allele Identifier: CA379960573
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1966950
ClinVar RCV Id: RCV002721677
dbSNP Id: rs1590345490

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32400046T>C , CM000673.2:g.32400046T>C GRCh38
NC_000011.9:g.32421592T>C , CM000673.1:g.32421592T>C GRCh37
NC_000011.8:g.32378168T>C NCBI36
NG_009272.1:g.40496A>G , LRG_525:g.40496A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.966-2A>G ENSP00000331327.5:n.966-2A>G
ENST00000379077.9:c.*201-2A>G ENSP00000368368.5:n.*201-2A>G
ENST00000379079.8:c.366-2A>G ENSP00000368370.2:n.366-2A>G
ENST00000448076.9:c.1017-2A>G ENSP00000413452.5:n.1017-2A>G
ENST00000452863.10:c.1017-2A>G MANE Select ENSP00000415516.5:n.1017-2A>G
ENST00000526685.2:n.471-2A>G
ENST00000639563.3:c.966-2A>G ENSP00000492269.3:n.966-2A>G
ENST00000639907.2:n.158A>G
ENST00000640146.2:c.342-2A>G ENSP00000491984.2:n.342-2A>G
ENST00000651794.1:n.760-2A>G
ENST00000652579.1:n.177-2A>G
ENST00000652724.1:n.207-2A>G
ENST00000332351.7:c.1002-2A>G ENSP00000331327.3:n.1002-2A>G
ENST00000379077.7:c.*201-2A>G ENSP00000368368.3:n.*201-2A>G
ENST00000379079.6:c.366-2A>G ENSP00000368370.2:n.366-2A>G
ENST00000448076.7:c.1002-2A>G ENSP00000413452.3:n.1002-2A>G
ENST00000452863.7:c.951-2A>G ENSP00000415516.3:n.951-2A>G
ENST00000526685.1:c.-172-2A>G ENSP00000436292.1:n.-172-2A>G
ENST00000527775.1:c.255-2A>G ENSP00000435351.1:n.255-2A>G
ENST00000527882.5:c.73-2A>G
ENST00000530998.5:c.315-2A>G ENSP00000435307.1:n.315-2A>G
NM_000378.4:c.951-2A>G NP_000369.3:n.951-2A>G
NM_001198551.1:c.366-2A>G , LRG_525t2:c.366-2A>G NP_001185480.1:n.366-2A>G
NM_001198552.1:c.315-2A>G NP_001185481.1:n.315-2A>G
NM_024424.3:c.1002-2A>G NP_077742.2:n.1002-2A>G
NM_024426.4:c.1002-2A>G NP_077744.3:n.1002-2A>G
NM_000378.5:c.966-2A>G NP_000369.4:n.966-2A>G
NM_024424.4:c.1017-2A>G NP_077742.3:n.1017-2A>G
NM_024426.5:c.1017-2A>G NP_077744.4:n.1017-2A>G
NM_001367854.1:c.-172-2A>G NP_001354783.1:n.-172-2A>G
NR_160306.1:n.1349-2A>G
NM_000378.6:c.966-2A>G NP_000369.4:n.966-2A>G
NM_001198552.2:c.315-2A>G NP_001185481.1:n.315-2A>G
NM_024424.5:c.1017-2A>G NP_077742.3:n.1017-2A>G
NM_024426.6:c.1017-2A>G MANE Select NP_077744.4:n.1017-2A>G