Canonical Allele Identifier: CA064583

Gene: WT1

Linked Data

• ClinVar Variation Id: 414073
• ClinVar RCV Id: RCV000464731 ; RCV002256290 ; RCV002496811 ; RCV004002125
• dbSNP Id: rs185744719
• ExAC: 11:32410735 C / T
• gnomAD v2: 11-32410735-C-T
• gnomAD v3: 11-32389189-C-T
• gnomAD v4: 11-32389189-C-T
• MyVariant Identifiers: chr11:g.32410735C>T (hg19) ; chr11:g.32389189C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32389189C>T , CM000673.2:g.32389189C>T	GRCh38
NC_000011.9:g.32410735C>T , CM000673.1:g.32410735C>T	GRCh37
NC_000011.8:g.32367311C>T	NCBI36
NG_009272.1:g.51353G>A , LRG_525:g.51353G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1388-10G>A	ENSP00000331327.5:n.1388-10G>A
ENST00000379077.9:c.*632-10G>A	ENSP00000368368.5:n.*632-10G>A
ENST00000379079.8:c.788-10G>A	ENSP00000368370.2:n.788-10G>A
ENST00000448076.9:c.1439-10G>A	ENSP00000413452.5:n.1439-10G>A
ENST00000452863.10:c.1448-10G>A MANE Select	ENSP00000415516.5:n.1448-10G>A
ENST00000526685.2:n.893-10G>A
ENST00000639563.3:c.1397-10G>A	ENSP00000492269.3:n.1397-10G>A
ENST00000639907.2:n.582-10G>A
ENST00000640146.2:c.773-10G>A	ENSP00000491984.2:n.773-10G>A
ENST00000650745.1:n.1258-10G>A
ENST00000650861.1:n.2020-10G>A
ENST00000650986.1:n.111-10G>A
ENST00000651459.1:c.219-10G>A
ENST00000651533.1:n.485-10G>A
ENST00000651668.1:n.385-10G>A
ENST00000651794.1:n.1291-10G>A
ENST00000651819.1:n.373-10G>A
ENST00000652579.1:n.708-10G>A
ENST00000652724.1:n.638-10G>A
ENST00000332351.7:c.1433-10G>A	ENSP00000331327.3:n.1433-10G>A
ENST00000379077.7:c.*632-10G>A	ENSP00000368368.3:n.*632-10G>A
ENST00000379079.6:c.788-10G>A	ENSP00000368370.2:n.788-10G>A
ENST00000448076.7:c.1424-10G>A	ENSP00000413452.3:n.1424-10G>A
ENST00000452863.7:c.1373-10G>A	ENSP00000415516.3:n.1373-10G>A
ENST00000527882.5:c.414-10G>A
ENST00000530998.5:c.746-10G>A	ENSP00000435307.1:n.746-10G>A
NM_000378.4:c.1373-10G>A	NP_000369.3:n.1373-10G>A
NM_001198551.1:c.788-10G>A , LRG_525t2:c.788-10G>A	NP_001185480.1:n.788-10G>A
NM_001198552.1:c.746-10G>A	NP_001185481.1:n.746-10G>A
NM_024424.3:c.1424-10G>A	NP_077742.2:n.1424-10G>A
NM_024426.4:c.1433-10G>A	NP_077744.3:n.1433-10G>A
NM_000378.5:c.1388-10G>A	NP_000369.4:n.1388-10G>A
NM_024424.4:c.1439-10G>A	NP_077742.3:n.1439-10G>A
NM_024426.5:c.1448-10G>A	NP_077744.4:n.1448-10G>A
NM_001367854.1:c.260-10G>A	NP_001354783.1:n.260-10G>A
NR_160306.1:n.1780-10G>A
NM_000378.6:c.1388-10G>A	NP_000369.4:n.1388-10G>A
NM_001198552.2:c.746-10G>A	NP_001185481.1:n.746-10G>A
NM_024424.5:c.1439-10G>A	NP_077742.3:n.1439-10G>A
NM_024426.6:c.1448-10G>A MANE Select	NP_077744.4:n.1448-10G>A