Canonical Allele Identifier: CA379959151

Gene: WT1

Linked Data

• dbSNP Id: rs2132919588
• MyVariant Identifiers: chr11:g.32414223C>G (hg19) ; chr11:g.32392677C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392677C>G , CM000673.2:g.32392677C>G	GRCh38
NC_000011.9:g.32414223C>G , CM000673.1:g.32414223C>G	GRCh37
NC_000011.8:g.32370799C>G	NCBI36
NG_009272.1:g.47865G>C , LRG_525:g.47865G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1292G>C	ENSP00000331327.5:p.Arg431Thr
ENST00000379077.9:c.*527G>C	ENSP00000368368.5:n.*527G>C
ENST00000379079.8:c.692G>C	ENSP00000368370.2:p.Arg231Thr
ENST00000448076.9:c.1343G>C	ENSP00000413452.5:p.Arg448Thr
ENST00000452863.10:c.1343G>C MANE Select	ENSP00000415516.5:p.Arg448Thr
ENST00000526685.2:n.797G>C
ENST00000639563.3:c.1292G>C	ENSP00000492269.3:p.Arg431Thr
ENST00000639907.2:n.486G>C
ENST00000640146.2:c.668G>C	ENSP00000491984.2:p.Arg223Thr
ENST00000650745.1:n.552G>C
ENST00000650861.1:n.1924G>C
ENST00000651459.1:c.114G>C
ENST00000651533.1:n.389G>C
ENST00000651668.1:n.280G>C
ENST00000651794.1:n.1186G>C
ENST00000651819.1:n.268G>C
ENST00000652579.1:n.603G>C
ENST00000652724.1:n.533G>C
ENST00000332351.7:c.1328G>C	ENSP00000331327.3:p.Arg443Thr
ENST00000379077.7:c.*527G>C	ENSP00000368368.3:n.*527G>C
ENST00000379079.6:c.692G>C	ENSP00000368370.2:p.Arg231Thr
ENST00000448076.7:c.1328G>C	ENSP00000413452.3:p.Arg443Thr
ENST00000452863.7:c.1277G>C	ENSP00000415516.3:p.Arg426Thr
ENST00000527882.5:c.321-613G>C
ENST00000530998.5:c.641G>C	ENSP00000435307.1:p.Arg214Thr
NM_000378.4:c.1277G>C	NP_000369.3:p.Arg426Thr
NM_001198551.1:c.692G>C , LRG_525t2:c.692G>C	NP_001185480.1:p.Arg231Thr
NM_001198552.1:c.641G>C	NP_001185481.1:p.Arg214Thr
NM_024424.3:c.1328G>C	NP_077742.2:p.Arg443Thr
NM_024426.4:c.1328G>C	NP_077744.3:p.Arg443Thr
NM_000378.5:c.1292G>C	NP_000369.4:p.Arg431Thr
NM_024424.4:c.1343G>C	NP_077742.3:p.Arg448Thr
NM_024426.5:c.1343G>C	NP_077744.4:p.Arg448Thr
NM_001367854.1:c.155G>C	NP_001354783.1:p.Arg52Thr
NR_160306.1:n.1675G>C
NM_000378.6:c.1292G>C	NP_000369.4:p.Arg431Thr
NM_001198552.2:c.641G>C	NP_001185481.1:p.Arg214Thr
NM_024424.5:c.1343G>C	NP_077742.3:p.Arg448Thr
NM_024426.6:c.1343G>C MANE Select	NP_077744.4:p.Arg448Thr