Canonical Allele Identifier: CA016298

Gene: WT1

Linked Data

• ClinVar Variation Id: 3495
• ClinVar RCV Id: RCV000003667 ; RCV000003668 ; RCV002512715
• dbSNP Id: rs28942089
• MyVariant Identifiers: chr11:g.32414218G>A (hg19) ; chr11:g.32392672G>A (hg38)
• PubMed: PMID:1327525 ; PMID:9529364

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392672G>A , CM000673.2:g.32392672G>A	GRCh38
NC_000011.9:g.32414218G>A , CM000673.1:g.32414218G>A	GRCh37
NC_000011.8:g.32370794G>A	NCBI36
NG_009272.1:g.47870C>T , LRG_525:g.47870C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1297C>T	ENSP00000331327.5:p.His433Tyr
ENST00000379077.9:c.*532C>T	ENSP00000368368.5:n.*532C>T
ENST00000379079.8:c.697C>T	ENSP00000368370.2:p.His233Tyr
ENST00000448076.9:c.1348C>T	ENSP00000413452.5:p.His450Tyr
ENST00000452863.10:c.1348C>T MANE Select	ENSP00000415516.5:p.His450Tyr
ENST00000526685.2:n.802C>T
ENST00000639563.3:c.1297C>T	ENSP00000492269.3:p.His433Tyr
ENST00000639907.2:n.491C>T
ENST00000640146.2:c.673C>T	ENSP00000491984.2:p.His225Tyr
ENST00000650745.1:n.557C>T
ENST00000650861.1:n.1929C>T
ENST00000651459.1:c.119C>T
ENST00000651533.1:n.394C>T
ENST00000651668.1:n.285C>T
ENST00000651794.1:n.1191C>T
ENST00000651819.1:n.273C>T
ENST00000652579.1:n.608C>T
ENST00000652724.1:n.538C>T
ENST00000332351.7:c.1333C>T	ENSP00000331327.3:p.His445Tyr
ENST00000379077.7:c.*532C>T	ENSP00000368368.3:n.*532C>T
ENST00000379079.6:c.697C>T	ENSP00000368370.2:p.His233Tyr
ENST00000448076.7:c.1333C>T	ENSP00000413452.3:p.His445Tyr
ENST00000452863.7:c.1282C>T	ENSP00000415516.3:p.His428Tyr
ENST00000527882.5:c.321-608C>T
ENST00000530998.5:c.646C>T	ENSP00000435307.1:p.His216Tyr
NM_000378.4:c.1282C>T	NP_000369.3:p.His428Tyr
NM_001198551.1:c.697C>T , LRG_525t2:c.697C>T	NP_001185480.1:p.His233Tyr
NM_001198552.1:c.646C>T	NP_001185481.1:p.His216Tyr
NM_024424.3:c.1333C>T	NP_077742.2:p.His445Tyr
NM_024426.4:c.1333C>T	NP_077744.3:p.His445Tyr
NM_000378.5:c.1297C>T	NP_000369.4:p.His433Tyr
NM_024424.4:c.1348C>T	NP_077742.3:p.His450Tyr
NM_024426.5:c.1348C>T	NP_077744.4:p.His450Tyr
NM_001367854.1:c.160C>T	NP_001354783.1:p.His54Tyr
NR_160306.1:n.1680C>T
NM_000378.6:c.1297C>T	NP_000369.4:p.His433Tyr
NM_001198552.2:c.646C>T	NP_001185481.1:p.His216Tyr
NM_024424.5:c.1348C>T	NP_077742.3:p.His450Tyr
NM_024426.6:c.1348C>T MANE Select	NP_077744.4:p.His450Tyr