Canonical Allele Identifier: CA379957492

Gene: WT1

Linked Data

• ClinVar Variation Id: 476692
• ClinVar RCV Id: RCV000527759
• dbSNP Id: rs1554938531
• MyVariant Identifiers: chr11:g.32410632T>A (hg19) ; chr11:g.32389086T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32389086T>A , CM000673.2:g.32389086T>A	GRCh38
NC_000011.9:g.32410632T>A , CM000673.1:g.32410632T>A	GRCh37
NC_000011.8:g.32367208T>A	NCBI36
NG_009272.1:g.51456A>T , LRG_525:g.51456A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1481A>T	ENSP00000331327.5:p.Asn494Ile
ENST00000379077.9:c.*725A>T	ENSP00000368368.5:n.*725A>T
ENST00000379079.8:c.881A>T	ENSP00000368370.2:p.Asn294Ile
ENST00000448076.9:c.1532A>T	ENSP00000413452.5:p.Asn511Ile
ENST00000452863.10:c.1541A>T MANE Select	ENSP00000415516.5:p.Asn514Ile
ENST00000639563.3:c.1490A>T	ENSP00000492269.3:p.Asn497Ile
ENST00000639907.2:n.675A>T
ENST00000640146.2:c.866A>T	ENSP00000491984.2:p.Asn289Ile
ENST00000650745.1:n.1351A>T
ENST00000650861.1:n.2113A>T
ENST00000650986.1:n.204A>T
ENST00000651459.1:c.312A>T
ENST00000651533.1:n.578A>T
ENST00000651668.1:n.478A>T
ENST00000651794.1:n.1384A>T
ENST00000651819.1:n.466A>T
ENST00000652579.1:n.801A>T
ENST00000652724.1:n.731A>T
ENST00000332351.7:c.1526A>T	ENSP00000331327.3:p.Asn509Ile
ENST00000379077.7:c.*725A>T	ENSP00000368368.3:n.*725A>T
ENST00000379079.6:c.881A>T	ENSP00000368370.2:p.Asn294Ile
ENST00000448076.7:c.1517A>T	ENSP00000413452.3:p.Asn506Ile
ENST00000452863.7:c.1466A>T	ENSP00000415516.3:p.Asn489Ile
ENST00000527882.5:c.507A>T
ENST00000530998.5:c.839A>T	ENSP00000435307.1:p.Asn280Ile
NM_000378.4:c.1466A>T	NP_000369.3:p.Asn489Ile
NM_001198551.1:c.881A>T , LRG_525t2:c.881A>T	NP_001185480.1:p.Asn294Ile
NM_001198552.1:c.839A>T	NP_001185481.1:p.Asn280Ile
NM_024424.3:c.1517A>T	NP_077742.2:p.Asn506Ile
NM_024426.4:c.1526A>T	NP_077744.3:p.Asn509Ile
NM_000378.5:c.1481A>T	NP_000369.4:p.Asn494Ile
NM_024424.4:c.1532A>T	NP_077742.3:p.Asn511Ile
NM_024426.5:c.1541A>T	NP_077744.4:p.Asn514Ile
NM_001367854.1:c.353A>T	NP_001354783.1:p.Asn118Ile
NR_160306.1:n.1873A>T
NM_000378.6:c.1481A>T	NP_000369.4:p.Asn494Ile
NM_001198552.2:c.839A>T	NP_001185481.1:p.Asn280Ile
NM_024424.5:c.1532A>T	NP_077742.3:p.Asn511Ile
NM_024426.6:c.1541A>T MANE Select	NP_077744.4:p.Asn514Ile