Canonical Allele Identifier: CA1139661878

Gene: WT1

Linked Data

• ClinVar Variation Id: 941959
• ClinVar RCV Id: RCV001211841
• dbSNP Id: rs1852720933

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417663A>T , CM000673.2:g.32417663A>T	GRCh38
NC_000011.9:g.32439209A>T , CM000673.1:g.32439209A>T	GRCh37
NC_000011.8:g.32395785A>T	NCBI36
NG_009272.1:g.22879T>A , LRG_525:g.22879T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.888-9T>A	ENSP00000331327.5:n.888-9T>A
ENST00000379077.9:c.888-9T>A	ENSP00000368368.5:n.888-9T>A
ENST00000379079.8:c.237-9T>A	ENSP00000368370.2:n.237-9T>A
ENST00000448076.9:c.888-9T>A	ENSP00000413452.5:n.888-9T>A
ENST00000452863.10:c.888-9T>A MANE Select	ENSP00000415516.5:n.888-9T>A
ENST00000639563.3:c.888-9T>A	ENSP00000492269.3:n.888-9T>A
ENST00000640146.2:c.264-9T>A	ENSP00000491984.2:n.264-9T>A
ENST00000332351.7:c.873-9T>A	ENSP00000331327.3:n.873-9T>A
ENST00000379077.7:c.873-9T>A	ENSP00000368368.3:n.873-9T>A
ENST00000379079.6:c.237-9T>A	ENSP00000368370.2:n.237-9T>A
ENST00000448076.7:c.873-9T>A	ENSP00000413452.3:n.873-9T>A
ENST00000452863.7:c.873-9T>A	ENSP00000415516.3:n.873-9T>A
ENST00000527775.1:c.126-9T>A	ENSP00000435351.1:n.126-9T>A
ENST00000530998.5:c.237-9T>A	ENSP00000435307.1:n.237-9T>A
NM_000378.4:c.873-9T>A	NP_000369.3:n.873-9T>A
NM_001198551.1:c.237-9T>A , LRG_525t2:c.237-9T>A	NP_001185480.1:n.237-9T>A
NM_001198552.1:c.237-9T>A	NP_001185481.1:n.237-9T>A
NM_024424.3:c.873-9T>A	NP_077742.2:n.873-9T>A
NM_024426.4:c.873-9T>A	NP_077744.3:n.873-9T>A
NM_000378.5:c.888-9T>A	NP_000369.4:n.888-9T>A
NM_024424.4:c.888-9T>A	NP_077742.3:n.888-9T>A
NM_024426.5:c.888-9T>A	NP_077744.4:n.888-9T>A
NR_160306.1:n.1067-9T>A
NM_000378.6:c.888-9T>A	NP_000369.4:n.888-9T>A
NM_001198552.2:c.237-9T>A	NP_001185481.1:n.237-9T>A
NM_024424.5:c.888-9T>A	NP_077742.3:n.888-9T>A
NM_024426.6:c.888-9T>A MANE Select	NP_077744.4:n.888-9T>A