Canonical Allele Identifier: CA658797607

Gene: WT1

Linked Data

• ClinVar Variation Id: 543120
• ClinVar RCV Id: RCV000653783
• dbSNP Id: rs1554939839
• MyVariant Identifiers: chr11:g.32417918del (hg19) ; chr11:g.32396372del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396373del , CM000673.2:g.32396373del	GRCh38
NC_000011.9:g.32417919del , CM000673.1:g.32417919del	GRCh37
NC_000011.8:g.32374495del	NCBI36
NG_009272.1:g.44170del , LRG_525:g.44170del

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1098del	ENSP00000331327.5:p.Val367TyrfsTer?
ENST00000379077.9:c.*333del	ENSP00000368368.5:n.*333del
ENST00000379079.8:c.498del	ENSP00000368370.2:p.Val167TyrfsTer?
ENST00000448076.9:c.1149del	ENSP00000413452.5:p.Val384TyrfsTer?
ENST00000452863.10:c.1149del MANE Select	ENSP00000415516.5:p.Val384TyrfsTer?
ENST00000526685.2:n.603del
ENST00000639563.3:c.1098del	ENSP00000492269.3:p.Val367TyrfsTer?
ENST00000639907.2:n.292del
ENST00000640146.2:c.474del	ENSP00000491984.2:p.Val159TyrfsTer?
ENST00000650861.1:n.1730del
ENST00000651459.1:c.35+3576del
ENST00000651668.1:n.86del
ENST00000651794.1:n.892del
ENST00000651819.1:n.74del
ENST00000652579.1:n.309del
ENST00000652724.1:n.339del
ENST00000332351.7:c.1134del	ENSP00000331327.3:p.Val379TyrfsTer?
ENST00000379077.7:c.*333del	ENSP00000368368.3:n.*333del
ENST00000379079.6:c.498del	ENSP00000368370.2:p.Val167TyrfsTer?
ENST00000448076.7:c.1134del	ENSP00000413452.3:p.Val379TyrfsTer?
ENST00000452863.7:c.1083del	ENSP00000415516.3:p.Val362TyrfsTer?
ENST00000526685.1:c.-40del	ENSP00000436292.1:n.-40del
ENST00000527775.1:c.387del	ENSP00000435351.1:p.Val130TyrfsTer?
ENST00000527882.5:c.205del
ENST00000530998.5:c.447del	ENSP00000435307.1:p.Val150TyrfsTer?
NM_000378.4:c.1083del	NP_000369.3:p.Val362TyrfsTer?
NM_001198551.1:c.498del , LRG_525t2:c.498del	NP_001185480.1:p.Val167TyrfsTer?
NM_001198552.1:c.447del	NP_001185481.1:p.Val150TyrfsTer?
NM_024424.3:c.1134del	NP_077742.2:p.Val379TyrfsTer?
NM_024426.4:c.1134del	NP_077744.3:p.Val379TyrfsTer?
NM_000378.5:c.1098del	NP_000369.4:p.Val367TyrfsTer?
NM_024424.4:c.1149del	NP_077742.3:p.Val384TyrfsTer?
NM_024426.5:c.1149del	NP_077744.4:p.Val384TyrfsTer?
NM_001367854.1:c.-40del	NP_001354783.1:n.-40del
NR_160306.1:n.1481del
NM_000378.6:c.1098del	NP_000369.4:p.Val367TyrfsTer?
NM_001198552.2:c.447del	NP_001185481.1:p.Val150TyrfsTer?
NM_024424.5:c.1149del	NP_077742.3:p.Val384TyrfsTer?
NM_024426.6:c.1149del MANE Select	NP_077744.4:p.Val384TyrfsTer?