Canonical Allele Identifier: CA10634653

Gene: WT1

Linked Data

• ClinVar Variation Id: 304401
• ClinVar RCV Id: RCV000298577 ; RCV000334858 ; RCV000338201 ; RCV000406182
• dbSNP Id: rs142726499
• gnomAD v2: 11-32410062-C-T
• gnomAD v3: 11-32388516-C-T
• gnomAD v4: 11-32388516-C-T
• MyVariant Identifiers: chr11:g.32410062C>T (hg19) ; chr11:g.32388516C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32388516C>T , CM000673.2:g.32388516C>T	GRCh38
NC_000011.9:g.32410062C>T , CM000673.1:g.32410062C>T	GRCh37
NC_000011.8:g.32366638C>T	NCBI36
NG_009272.1:g.52026G>A , LRG_525:g.52026G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.*542G>A	ENSP00000331327.5:n.*542G>A
ENST00000379077.9:c.*1295G>A	ENSP00000368368.5:n.*1295G>A
ENST00000379079.8:c.*542G>A	ENSP00000368370.2:n.*542G>A
ENST00000452863.10:c.*542G>A MANE Select	ENSP00000415516.5:n.*542G>A
ENST00000639907.2:n.1245G>A
ENST00000640146.2:c.*542G>A	ENSP00000491984.2:n.*542G>A
ENST00000650745.1:n.1921G>A
ENST00000650861.1:n.2683G>A
ENST00000651459.1:c.882G>A
ENST00000651533.1:n.1148G>A
ENST00000651668.1:n.1048G>A
ENST00000651794.1:n.1954G>A
ENST00000651819.1:n.1036G>A
ENST00000652579.1:n.1371G>A
ENST00000652724.1:n.1301G>A
ENST00000332351.7:c.*542G>A	ENSP00000331327.3:n.*542G>A
ENST00000379077.7:c.*1295G>A	ENSP00000368368.3:n.*1295G>A
ENST00000379079.6:c.*542G>A	ENSP00000368370.2:n.*542G>A
ENST00000452863.7:c.2036G>A	ENSP00000415516.3:n.2036G>A
ENST00000530998.5:c.*542G>A	ENSP00000435307.1:n.*542G>A
NM_000378.4:c.*542G>A	NP_000369.3:n.*542G>A
NM_001198551.1:c.*542G>A , LRG_525t2:c.*542G>A	NP_001185480.1:n.*542G>A
NM_001198552.1:c.*542G>A	NP_001185481.1:n.*542G>A
NM_024424.3:c.*542G>A	NP_077742.2:n.*542G>A
NM_024426.4:c.*542G>A	NP_077744.3:n.*542G>A
NM_000378.5:c.*542G>A	NP_000369.4:n.*542G>A
NM_024424.4:c.*542G>A	NP_077742.3:n.*542G>A
NM_024426.5:c.*542G>A	NP_077744.4:n.*542G>A
NM_001367854.1:c.*542G>A	NP_001354783.1:n.*542G>A
NR_160306.1:n.2443G>A
NM_000378.6:c.*542G>A	NP_000369.4:n.*542G>A
NM_001198552.2:c.*542G>A	NP_001185481.1:n.*542G>A
NM_024424.5:c.*542G>A	NP_077742.3:n.*542G>A
NM_024426.6:c.*542G>A MANE Select	NP_077744.4:n.*542G>A