Canonical Allele Identifier: CA379957502

Gene: WT1

Linked Data

• ClinVar Variation Id: 476691
• ClinVar RCV Id: RCV000556002
• dbSNP Id: rs1363144688
• MyVariant Identifiers: chr11:g.32410635C>G (hg19) ; chr11:g.32389089C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32389089C>G , CM000673.2:g.32389089C>G	GRCh38
NC_000011.9:g.32410635C>G , CM000673.1:g.32410635C>G	GRCh37
NC_000011.8:g.32367211C>G	NCBI36
NG_009272.1:g.51453G>C , LRG_525:g.51453G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1478G>C	ENSP00000331327.5:p.Arg493Thr
ENST00000379077.9:c.*722G>C	ENSP00000368368.5:n.*722G>C
ENST00000379079.8:c.878G>C	ENSP00000368370.2:p.Arg293Thr
ENST00000448076.9:c.1529G>C	ENSP00000413452.5:p.Arg510Thr
ENST00000452863.10:c.1538G>C MANE Select	ENSP00000415516.5:p.Arg513Thr
ENST00000639563.3:c.1487G>C	ENSP00000492269.3:p.Arg496Thr
ENST00000639907.2:n.672G>C
ENST00000640146.2:c.863G>C	ENSP00000491984.2:p.Arg288Thr
ENST00000650745.1:n.1348G>C
ENST00000650861.1:n.2110G>C
ENST00000650986.1:n.201G>C
ENST00000651459.1:c.309G>C
ENST00000651533.1:n.575G>C
ENST00000651668.1:n.475G>C
ENST00000651794.1:n.1381G>C
ENST00000651819.1:n.463G>C
ENST00000652579.1:n.798G>C
ENST00000652724.1:n.728G>C
ENST00000332351.7:c.1523G>C	ENSP00000331327.3:p.Arg508Thr
ENST00000379077.7:c.*722G>C	ENSP00000368368.3:n.*722G>C
ENST00000379079.6:c.878G>C	ENSP00000368370.2:p.Arg293Thr
ENST00000448076.7:c.1514G>C	ENSP00000413452.3:p.Arg505Thr
ENST00000452863.7:c.1463G>C	ENSP00000415516.3:p.Arg488Thr
ENST00000527882.5:c.504G>C
ENST00000530998.5:c.836G>C	ENSP00000435307.1:p.Arg279Thr
NM_000378.4:c.1463G>C	NP_000369.3:p.Arg488Thr
NM_001198551.1:c.878G>C , LRG_525t2:c.878G>C	NP_001185480.1:p.Arg293Thr
NM_001198552.1:c.836G>C	NP_001185481.1:p.Arg279Thr
NM_024424.3:c.1514G>C	NP_077742.2:p.Arg505Thr
NM_024426.4:c.1523G>C	NP_077744.3:p.Arg508Thr
NM_000378.5:c.1478G>C	NP_000369.4:p.Arg493Thr
NM_024424.4:c.1529G>C	NP_077742.3:p.Arg510Thr
NM_024426.5:c.1538G>C	NP_077744.4:p.Arg513Thr
NM_001367854.1:c.350G>C	NP_001354783.1:p.Arg117Thr
NR_160306.1:n.1870G>C
NM_000378.6:c.1478G>C	NP_000369.4:p.Arg493Thr
NM_001198552.2:c.836G>C	NP_001185481.1:p.Arg279Thr
NM_024424.5:c.1529G>C	NP_077742.3:p.Arg510Thr
NM_024426.6:c.1538G>C MANE Select	NP_077744.4:p.Arg513Thr