Canonical Allele Identifier: CA016265

Gene: WT1

Linked Data

• ClinVar Variation Id: 3496
• ClinVar RCV Id: RCV000003669 ; RCV002512716
• dbSNP Id: rs121907905
• MyVariant Identifiers: chr11:g.32414269A>C (hg19) ; chr11:g.32392723A>C (hg38)
• PubMed: PMID:9090524

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392723A>C , CM000673.2:g.32392723A>C	GRCh38
NC_000011.9:g.32414269A>C , CM000673.1:g.32414269A>C	GRCh37
NC_000011.8:g.32370845A>C	NCBI36
NG_009272.1:g.47819T>G , LRG_525:g.47819T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1246T>G	ENSP00000331327.5:p.Cys416Gly
ENST00000379077.9:c.*481T>G	ENSP00000368368.5:n.*481T>G
ENST00000379079.8:c.646T>G	ENSP00000368370.2:p.Cys216Gly
ENST00000448076.9:c.1297T>G	ENSP00000413452.5:p.Cys433Gly
ENST00000452863.10:c.1297T>G MANE Select	ENSP00000415516.5:p.Cys433Gly
ENST00000526685.2:n.751T>G
ENST00000639563.3:c.1246T>G	ENSP00000492269.3:p.Cys416Gly
ENST00000639907.2:n.440T>G
ENST00000640146.2:c.622T>G	ENSP00000491984.2:p.Cys208Gly
ENST00000650745.1:n.506T>G
ENST00000650861.1:n.1878T>G
ENST00000651459.1:c.68T>G
ENST00000651533.1:n.343T>G
ENST00000651668.1:n.234T>G
ENST00000651794.1:n.1140T>G
ENST00000651819.1:n.222T>G
ENST00000652579.1:n.557T>G
ENST00000652724.1:n.487T>G
ENST00000332351.7:c.1282T>G	ENSP00000331327.3:p.Cys428Gly
ENST00000379077.7:c.*481T>G	ENSP00000368368.3:n.*481T>G
ENST00000379079.6:c.646T>G	ENSP00000368370.2:p.Cys216Gly
ENST00000448076.7:c.1282T>G	ENSP00000413452.3:p.Cys428Gly
ENST00000452863.7:c.1231T>G	ENSP00000415516.3:p.Cys411Gly
ENST00000527882.5:c.321-659T>G
ENST00000530998.5:c.595T>G	ENSP00000435307.1:p.Cys199Gly
NM_000378.4:c.1231T>G	NP_000369.3:p.Cys411Gly
NM_001198551.1:c.646T>G , LRG_525t2:c.646T>G	NP_001185480.1:p.Cys216Gly
NM_001198552.1:c.595T>G	NP_001185481.1:p.Cys199Gly
NM_024424.3:c.1282T>G	NP_077742.2:p.Cys428Gly
NM_024426.4:c.1282T>G	NP_077744.3:p.Cys428Gly
NM_000378.5:c.1246T>G	NP_000369.4:p.Cys416Gly
NM_024424.4:c.1297T>G	NP_077742.3:p.Cys433Gly
NM_024426.5:c.1297T>G	NP_077744.4:p.Cys433Gly
NM_001367854.1:c.109T>G	NP_001354783.1:p.Cys37Gly
NR_160306.1:n.1629T>G
NM_000378.6:c.1246T>G	NP_000369.4:p.Cys416Gly
NM_001198552.2:c.595T>G	NP_001185481.1:p.Cys199Gly
NM_024424.5:c.1297T>G	NP_077742.3:p.Cys433Gly
NM_024426.6:c.1297T>G MANE Select	NP_077744.4:p.Cys433Gly