Canonical Allele Identifier: CA016273

Gene: WT1

Linked Data

• ClinVar Variation Id: 3497
• ClinVar RCV Id: RCV000003670 ; RCV000003671 ; RCV000685465 ; RCV000762840
• dbSNP Id: rs121907906
• COSMIC: COSM21401 ; COSM5879212 ; COSM5879213
• MyVariant Identifiers: chr11:g.32414263G>A (hg19) ; chr11:g.32392717G>A (hg38)
• PubMed: PMID:8975729 ; PMID:9090524

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392717G>A , CM000673.2:g.32392717G>A	GRCh38
NC_000011.9:g.32414263G>A , CM000673.1:g.32414263G>A	GRCh37
NC_000011.8:g.32370839G>A	NCBI36
NG_009272.1:g.47825C>T , LRG_525:g.47825C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1252C>T	ENSP00000331327.5:p.Arg418Ter
ENST00000379077.9:c.*487C>T	ENSP00000368368.5:n.*487C>T
ENST00000379079.8:c.652C>T	ENSP00000368370.2:p.Arg218Ter
ENST00000448076.9:c.1303C>T	ENSP00000413452.5:p.Arg435Ter
ENST00000452863.10:c.1303C>T MANE Select	ENSP00000415516.5:p.Arg435Ter
ENST00000526685.2:n.757C>T
ENST00000639563.3:c.1252C>T	ENSP00000492269.3:p.Arg418Ter
ENST00000639907.2:n.446C>T
ENST00000640146.2:c.628C>T	ENSP00000491984.2:p.Arg210Ter
ENST00000650745.1:n.512C>T
ENST00000650861.1:n.1884C>T
ENST00000651459.1:c.74C>T
ENST00000651533.1:n.349C>T
ENST00000651668.1:n.240C>T
ENST00000651794.1:n.1146C>T
ENST00000651819.1:n.228C>T
ENST00000652579.1:n.563C>T
ENST00000652724.1:n.493C>T
ENST00000332351.7:c.1288C>T	ENSP00000331327.3:p.Arg430Ter
ENST00000379077.7:c.*487C>T	ENSP00000368368.3:n.*487C>T
ENST00000379079.6:c.652C>T	ENSP00000368370.2:p.Arg218Ter
ENST00000448076.7:c.1288C>T	ENSP00000413452.3:p.Arg430Ter
ENST00000452863.7:c.1237C>T	ENSP00000415516.3:p.Arg413Ter
ENST00000527882.5:c.321-653C>T
ENST00000530998.5:c.601C>T	ENSP00000435307.1:p.Arg201Ter
NM_000378.4:c.1237C>T	NP_000369.3:p.Arg413Ter
NM_001198551.1:c.652C>T , LRG_525t2:c.652C>T	NP_001185480.1:p.Arg218Ter
NM_001198552.1:c.601C>T	NP_001185481.1:p.Arg201Ter
NM_024424.3:c.1288C>T	NP_077742.2:p.Arg430Ter
NM_024426.4:c.1288C>T	NP_077744.3:p.Arg430Ter
NM_000378.5:c.1252C>T	NP_000369.4:p.Arg418Ter
NM_024424.4:c.1303C>T	NP_077742.3:p.Arg435Ter
NM_024426.5:c.1303C>T	NP_077744.4:p.Arg435Ter
NM_001367854.1:c.115C>T	NP_001354783.1:p.Arg39Ter
NR_160306.1:n.1635C>T
NM_000378.6:c.1252C>T	NP_000369.4:p.Arg418Ter
NM_001198552.2:c.601C>T	NP_001185481.1:p.Arg201Ter
NM_024424.5:c.1303C>T	NP_077742.3:p.Arg435Ter
NM_024426.6:c.1303C>T MANE Select	NP_077744.4:p.Arg435Ter