Canonical Allele Identifier: CA10634643

Gene: WT1

Linked Data

• ClinVar Variation Id: 304391
• ClinVar RCV Id: RCV000339331 ; RCV000363480 ; RCV000393175
• dbSNP Id: rs886048214
• gnomAD v2: 11-32409819-G-T
• gnomAD v3: 11-32388273-G-T
• gnomAD v4: 11-32388273-G-T
• MyVariant Identifiers: chr11:g.32409819G>T (hg19) ; chr11:g.32388273G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32388273G>T , CM000673.2:g.32388273G>T	GRCh38
NC_000011.9:g.32409819G>T , CM000673.1:g.32409819G>T	GRCh37
NC_000011.8:g.32366395G>T	NCBI36
NG_009272.1:g.52269C>A , LRG_525:g.52269C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.*785C>A	ENSP00000331327.5:n.*785C>A
ENST00000379077.9:c.*1538C>A	ENSP00000368368.5:n.*1538C>A
ENST00000379079.8:c.*785C>A	ENSP00000368370.2:n.*785C>A
ENST00000452863.10:c.*785C>A MANE Select	ENSP00000415516.5:n.*785C>A
ENST00000639907.2:n.1488C>A
ENST00000640146.2:c.*785C>A	ENSP00000491984.2:n.*785C>A
ENST00000650745.1:n.2164C>A
ENST00000650861.1:n.2926C>A
ENST00000651533.1:n.1391C>A
ENST00000651668.1:n.1291C>A
ENST00000651794.1:n.2197C>A
ENST00000651819.1:n.1279C>A
ENST00000652579.1:n.1614C>A
ENST00000652724.1:n.1544C>A
ENST00000332351.7:c.*785C>A	ENSP00000331327.3:n.*785C>A
ENST00000379077.7:c.*1538C>A	ENSP00000368368.3:n.*1538C>A
ENST00000379079.6:c.*785C>A	ENSP00000368370.2:n.*785C>A
ENST00000452863.7:c.2279C>A	ENSP00000415516.3:n.2279C>A
ENST00000530998.5:c.*785C>A	ENSP00000435307.1:n.*785C>A
NM_000378.4:c.*785C>A	NP_000369.3:n.*785C>A
NM_001198551.1:c.*785C>A , LRG_525t2:c.*785C>A	NP_001185480.1:n.*785C>A
NM_001198552.1:c.*785C>A	NP_001185481.1:n.*785C>A
NM_024424.3:c.*785C>A	NP_077742.2:n.*785C>A
NM_024426.4:c.*785C>A	NP_077744.3:n.*785C>A
NM_000378.5:c.*785C>A	NP_000369.4:n.*785C>A
NM_024424.4:c.*785C>A	NP_077742.3:n.*785C>A
NM_024426.5:c.*785C>A	NP_077744.4:n.*785C>A
NM_001367854.1:c.*785C>A	NP_001354783.1:n.*785C>A
NR_160306.1:n.2686C>A
NM_000378.6:c.*785C>A	NP_000369.4:n.*785C>A
NM_001198552.2:c.*785C>A	NP_001185481.1:n.*785C>A
NM_024424.5:c.*785C>A	NP_077742.3:n.*785C>A
NM_024426.6:c.*785C>A MANE Select	NP_077744.4:n.*785C>A