Canonical Allele Identifier: CA064487

Gene: WT1

Linked Data

• ClinVar Variation Id: 2203509
• ClinVar RCV Id: RCV002651799
• dbSNP Id: rs752854428
• ExAC: 11:32413629 T / A
• gnomAD v2: 11-32413629-T-A
• gnomAD v4: 11-32392083-T-A
• MyVariant Identifiers: chr11:g.32413629T>A (hg19) ; chr11:g.32392083T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392083T>A , CM000673.2:g.32392083T>A	GRCh38
NC_000011.9:g.32413629T>A , CM000673.1:g.32413629T>A	GRCh37
NC_000011.8:g.32370205T>A	NCBI36
NG_009272.1:g.48459A>T , LRG_525:g.48459A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1304-19A>T	ENSP00000331327.5:n.1304-19A>T
ENST00000379077.9:c.*539-19A>T	ENSP00000368368.5:n.*539-19A>T
ENST00000379079.8:c.704-19A>T	ENSP00000368370.2:n.704-19A>T
ENST00000448076.9:c.1355-19A>T	ENSP00000413452.5:n.1355-19A>T
ENST00000452863.10:c.1355-19A>T MANE Select	ENSP00000415516.5:n.1355-19A>T
ENST00000526685.2:n.809-19A>T
ENST00000639563.3:c.1304-19A>T	ENSP00000492269.3:n.1304-19A>T
ENST00000639907.2:n.498-19A>T
ENST00000640146.2:c.680-19A>T	ENSP00000491984.2:n.680-19A>T
ENST00000650745.1:n.1146A>T
ENST00000650861.1:n.1936-19A>T
ENST00000651459.1:c.126-19A>T
ENST00000651533.1:n.401-19A>T
ENST00000651668.1:n.292-19A>T
ENST00000651794.1:n.1198-19A>T
ENST00000651819.1:n.280-19A>T
ENST00000652579.1:n.615-19A>T
ENST00000652724.1:n.545-19A>T
ENST00000332351.7:c.1340-19A>T	ENSP00000331327.3:n.1340-19A>T
ENST00000379077.7:c.*539-19A>T	ENSP00000368368.3:n.*539-19A>T
ENST00000379079.6:c.704-19A>T	ENSP00000368370.2:n.704-19A>T
ENST00000448076.7:c.1340-19A>T	ENSP00000413452.3:n.1340-19A>T
ENST00000452863.7:c.1289-19A>T	ENSP00000415516.3:n.1289-19A>T
ENST00000527882.5:c.321-19A>T
ENST00000530998.5:c.653-19A>T	ENSP00000435307.1:n.653-19A>T
NM_000378.4:c.1289-19A>T	NP_000369.3:n.1289-19A>T
NM_001198551.1:c.704-19A>T , LRG_525t2:c.704-19A>T	NP_001185480.1:n.704-19A>T
NM_001198552.1:c.653-19A>T	NP_001185481.1:n.653-19A>T
NM_024424.3:c.1340-19A>T	NP_077742.2:n.1340-19A>T
NM_024426.4:c.1340-19A>T	NP_077744.3:n.1340-19A>T
NM_000378.5:c.1304-19A>T	NP_000369.4:n.1304-19A>T
NM_024424.4:c.1355-19A>T	NP_077742.3:n.1355-19A>T
NM_024426.5:c.1355-19A>T	NP_077744.4:n.1355-19A>T
NM_001367854.1:c.167-19A>T	NP_001354783.1:n.167-19A>T
NR_160306.1:n.1687-19A>T
NM_000378.6:c.1304-19A>T	NP_000369.4:n.1304-19A>T
NM_001198552.2:c.653-19A>T	NP_001185481.1:n.653-19A>T
NM_024424.5:c.1355-19A>T	NP_077742.3:n.1355-19A>T
NM_024426.6:c.1355-19A>T MANE Select	NP_077744.4:n.1355-19A>T