Canonical Allele Identifier: CA016330

Gene: WT1

Linked Data

• ClinVar Variation Id: 3491
• ClinVar RCV Id: RCV000003663 ; RCV004547456
• dbSNP Id: rs121907903
• COSMIC: COSM27291 ; COSM5424216 ; COSM5424217
• MyVariant Identifiers: chr11:g.32413565C>G (hg19) ; chr11:g.32392019C>G (hg38)
• PubMed: PMID:1302008

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392019C>G , CM000673.2:g.32392019C>G	GRCh38
NC_000011.9:g.32413565C>G , CM000673.1:g.32413565C>G	GRCh37
NC_000011.8:g.32370141C>G	NCBI36
NG_009272.1:g.48523G>C , LRG_525:g.48523G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1349G>C	ENSP00000331327.5:p.Arg450Pro
ENST00000379077.9:c.*584G>C	ENSP00000368368.5:n.*584G>C
ENST00000379079.8:c.749G>C	ENSP00000368370.2:p.Arg250Pro
ENST00000448076.9:c.1400G>C	ENSP00000413452.5:p.Arg467Pro
ENST00000452863.10:c.1400G>C MANE Select	ENSP00000415516.5:p.Arg467Pro
ENST00000526685.2:n.854G>C
ENST00000639563.3:c.1349G>C	ENSP00000492269.3:p.Arg450Pro
ENST00000639907.2:n.543G>C
ENST00000640146.2:c.725G>C	ENSP00000491984.2:p.Arg242Pro
ENST00000650745.1:n.1210G>C
ENST00000650861.1:n.1981G>C
ENST00000650986.1:n.63G>C
ENST00000651459.1:c.171G>C
ENST00000651533.1:n.446G>C
ENST00000651668.1:n.337G>C
ENST00000651794.1:n.1243G>C
ENST00000651819.1:n.325G>C
ENST00000652579.1:n.660G>C
ENST00000652724.1:n.590G>C
ENST00000332351.7:c.1385G>C	ENSP00000331327.3:p.Arg462Pro
ENST00000379077.7:c.*584G>C	ENSP00000368368.3:n.*584G>C
ENST00000379079.6:c.749G>C	ENSP00000368370.2:p.Arg250Pro
ENST00000448076.7:c.1385G>C	ENSP00000413452.3:p.Arg462Pro
ENST00000452863.7:c.1334G>C	ENSP00000415516.3:p.Arg445Pro
ENST00000527882.5:c.366G>C
ENST00000530998.5:c.698G>C	ENSP00000435307.1:p.Arg233Pro
NM_000378.4:c.1334G>C	NP_000369.3:p.Arg445Pro
NM_001198551.1:c.749G>C , LRG_525t2:c.749G>C	NP_001185480.1:p.Arg250Pro
NM_001198552.1:c.698G>C	NP_001185481.1:p.Arg233Pro
NM_024424.3:c.1385G>C	NP_077742.2:p.Arg462Pro
NM_024426.4:c.1385G>C	NP_077744.3:p.Arg462Pro
NM_000378.5:c.1349G>C	NP_000369.4:p.Arg450Pro
NM_024424.4:c.1400G>C	NP_077742.3:p.Arg467Pro
NM_024426.5:c.1400G>C	NP_077744.4:p.Arg467Pro
NM_001367854.1:c.212G>C	NP_001354783.1:p.Arg71Pro
NR_160306.1:n.1732G>C
NM_000378.6:c.1349G>C	NP_000369.4:p.Arg450Pro
NM_001198552.2:c.698G>C	NP_001185481.1:p.Arg233Pro
NM_024424.5:c.1400G>C	NP_077742.3:p.Arg467Pro
NM_024426.6:c.1400G>C MANE Select	NP_077744.4:p.Arg467Pro