Canonical Allele Identifier: CA379958962

Gene: WT1

Linked Data

• ClinVar Variation Id: 2137049
• ClinVar RCV Id: RCV003062358
• MyVariant Identifiers: chr11:g.32413593A>G (hg19) ; chr11:g.32392047A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392047A>G , CM000673.2:g.32392047A>G	GRCh38
NC_000011.9:g.32413593A>G , CM000673.1:g.32413593A>G	GRCh37
NC_000011.8:g.32370169A>G	NCBI36
NG_009272.1:g.48495T>C , LRG_525:g.48495T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1321T>C	ENSP00000331327.5:p.Cys441Arg
ENST00000379077.9:c.*556T>C	ENSP00000368368.5:n.*556T>C
ENST00000379079.8:c.721T>C	ENSP00000368370.2:p.Cys241Arg
ENST00000448076.9:c.1372T>C	ENSP00000413452.5:p.Cys458Arg
ENST00000452863.10:c.1372T>C MANE Select	ENSP00000415516.5:p.Cys458Arg
ENST00000526685.2:n.826T>C
ENST00000639563.3:c.1321T>C	ENSP00000492269.3:p.Cys441Arg
ENST00000639907.2:n.515T>C
ENST00000640146.2:c.697T>C	ENSP00000491984.2:p.Cys233Arg
ENST00000650745.1:n.1182T>C
ENST00000650861.1:n.1953T>C
ENST00000650986.1:n.35T>C
ENST00000651459.1:c.143T>C
ENST00000651533.1:n.418T>C
ENST00000651668.1:n.309T>C
ENST00000651794.1:n.1215T>C
ENST00000651819.1:n.297T>C
ENST00000652579.1:n.632T>C
ENST00000652724.1:n.562T>C
ENST00000332351.7:c.1357T>C	ENSP00000331327.3:p.Cys453Arg
ENST00000379077.7:c.*556T>C	ENSP00000368368.3:n.*556T>C
ENST00000379079.6:c.721T>C	ENSP00000368370.2:p.Cys241Arg
ENST00000448076.7:c.1357T>C	ENSP00000413452.3:p.Cys453Arg
ENST00000452863.7:c.1306T>C	ENSP00000415516.3:p.Cys436Arg
ENST00000527882.5:c.338T>C
ENST00000530998.5:c.670T>C	ENSP00000435307.1:p.Cys224Arg
NM_000378.4:c.1306T>C	NP_000369.3:p.Cys436Arg
NM_001198551.1:c.721T>C , LRG_525t2:c.721T>C	NP_001185480.1:p.Cys241Arg
NM_001198552.1:c.670T>C	NP_001185481.1:p.Cys224Arg
NM_024424.3:c.1357T>C	NP_077742.2:p.Cys453Arg
NM_024426.4:c.1357T>C	NP_077744.3:p.Cys453Arg
NM_000378.5:c.1321T>C	NP_000369.4:p.Cys441Arg
NM_024424.4:c.1372T>C	NP_077742.3:p.Cys458Arg
NM_024426.5:c.1372T>C	NP_077744.4:p.Cys458Arg
NM_001367854.1:c.184T>C	NP_001354783.1:p.Cys62Arg
NR_160306.1:n.1704T>C
NM_000378.6:c.1321T>C	NP_000369.4:p.Cys441Arg
NM_001198552.2:c.670T>C	NP_001185481.1:p.Cys224Arg
NM_024424.5:c.1372T>C	NP_077742.3:p.Cys458Arg
NM_024426.6:c.1372T>C MANE Select	NP_077744.4:p.Cys458Arg