Canonical Allele Identifier: CA354126

Gene: WT1

Linked Data

• ClinVar Variation Id: 224480
• ClinVar RCV Id: RCV000210056
• dbSNP Id: rs869312745
• gnomAD v4: 11-32392807-C-A
• MyVariant Identifiers: chr11:g.32414353C>A (hg19) ; chr11:g.32392807C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392807C>A , CM000673.2:g.32392807C>A	GRCh38
NC_000011.9:g.32414353C>A , CM000673.1:g.32414353C>A	GRCh37
NC_000011.8:g.32370929C>A	NCBI36
NG_009272.1:g.47735G>T , LRG_525:g.47735G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1214-52G>T	ENSP00000331327.5:n.1214-52G>T
ENST00000379077.9:c.*449-52G>T	ENSP00000368368.5:n.*449-52G>T
ENST00000379079.8:c.614-52G>T	ENSP00000368370.2:n.614-52G>T
ENST00000448076.9:c.1265-52G>T	ENSP00000413452.5:n.1265-52G>T
ENST00000452863.10:c.1265-52G>T MANE Select	ENSP00000415516.5:n.1265-52G>T
ENST00000526685.2:n.719-52G>T
ENST00000639563.3:c.1214-52G>T	ENSP00000492269.3:n.1214-52G>T
ENST00000639907.2:n.408-52G>T
ENST00000640146.2:c.590-52G>T	ENSP00000491984.2:n.590-52G>T
ENST00000650745.1:n.422G>T
ENST00000650861.1:n.1846-52G>T
ENST00000651459.1:c.36-52G>T
ENST00000651533.1:n.259G>T
ENST00000651668.1:n.202-52G>T
ENST00000651794.1:n.1108-52G>T
ENST00000651819.1:n.190-52G>T
ENST00000652579.1:n.525-52G>T
ENST00000652724.1:n.455-52G>T
ENST00000332351.7:c.1250-52G>T	ENSP00000331327.3:n.1250-52G>T
ENST00000379077.7:c.*449-52G>T	ENSP00000368368.3:n.*449-52G>T
ENST00000379079.6:c.614-52G>T	ENSP00000368370.2:n.614-52G>T
ENST00000448076.7:c.1250-52G>T	ENSP00000413452.3:n.1250-52G>T
ENST00000452863.7:c.1199-52G>T	ENSP00000415516.3:n.1199-52G>T
ENST00000527882.5:c.321-743G>T
ENST00000530998.5:c.563-52G>T	ENSP00000435307.1:n.563-52G>T
NM_000378.4:c.1199-52G>T	NP_000369.3:n.1199-52G>T
NM_001198551.1:c.614-52G>T , LRG_525t2:c.614-52G>T	NP_001185480.1:n.614-52G>T
NM_001198552.1:c.563-52G>T	NP_001185481.1:n.563-52G>T
NM_024424.3:c.1250-52G>T	NP_077742.2:n.1250-52G>T
NM_024426.4:c.1250-52G>T	NP_077744.3:n.1250-52G>T
NM_000378.5:c.1214-52G>T	NP_000369.4:n.1214-52G>T
NM_024424.4:c.1265-52G>T	NP_077742.3:n.1265-52G>T
NM_024426.5:c.1265-52G>T	NP_077744.4:n.1265-52G>T
NM_001367854.1:c.77-52G>T	NP_001354783.1:n.77-52G>T
NR_160306.1:n.1597-52G>T
NM_000378.6:c.1214-52G>T	NP_000369.4:n.1214-52G>T
NM_001198552.2:c.563-52G>T	NP_001185481.1:n.563-52G>T
NM_024424.5:c.1265-52G>T	NP_077742.3:n.1265-52G>T
NM_024426.6:c.1265-52G>T MANE Select	NP_077744.4:n.1265-52G>T