Canonical Allele Identifier: CA379959155

Gene: WT1

Linked Data

• dbSNP Id: rs2132919622
• MyVariant Identifiers: chr11:g.32414224T>A (hg19) ; chr11:g.32392678T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392678T>A , CM000673.2:g.32392678T>A	GRCh38
NC_000011.9:g.32414224T>A , CM000673.1:g.32414224T>A	GRCh37
NC_000011.8:g.32370800T>A	NCBI36
NG_009272.1:g.47864A>T , LRG_525:g.47864A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1291A>T	ENSP00000331327.5:p.Arg431Trp
ENST00000379077.9:c.*526A>T	ENSP00000368368.5:n.*526A>T
ENST00000379079.8:c.691A>T	ENSP00000368370.2:p.Arg231Trp
ENST00000448076.9:c.1342A>T	ENSP00000413452.5:p.Arg448Trp
ENST00000452863.10:c.1342A>T MANE Select	ENSP00000415516.5:p.Arg448Trp
ENST00000526685.2:n.796A>T
ENST00000639563.3:c.1291A>T	ENSP00000492269.3:p.Arg431Trp
ENST00000639907.2:n.485A>T
ENST00000640146.2:c.667A>T	ENSP00000491984.2:p.Arg223Trp
ENST00000650745.1:n.551A>T
ENST00000650861.1:n.1923A>T
ENST00000651459.1:c.113A>T
ENST00000651533.1:n.388A>T
ENST00000651668.1:n.279A>T
ENST00000651794.1:n.1185A>T
ENST00000651819.1:n.267A>T
ENST00000652579.1:n.602A>T
ENST00000652724.1:n.532A>T
ENST00000332351.7:c.1327A>T	ENSP00000331327.3:p.Arg443Trp
ENST00000379077.7:c.*526A>T	ENSP00000368368.3:n.*526A>T
ENST00000379079.6:c.691A>T	ENSP00000368370.2:p.Arg231Trp
ENST00000448076.7:c.1327A>T	ENSP00000413452.3:p.Arg443Trp
ENST00000452863.7:c.1276A>T	ENSP00000415516.3:p.Arg426Trp
ENST00000527882.5:c.321-614A>T
ENST00000530998.5:c.640A>T	ENSP00000435307.1:p.Arg214Trp
NM_000378.4:c.1276A>T	NP_000369.3:p.Arg426Trp
NM_001198551.1:c.691A>T , LRG_525t2:c.691A>T	NP_001185480.1:p.Arg231Trp
NM_001198552.1:c.640A>T	NP_001185481.1:p.Arg214Trp
NM_024424.3:c.1327A>T	NP_077742.2:p.Arg443Trp
NM_024426.4:c.1327A>T	NP_077744.3:p.Arg443Trp
NM_000378.5:c.1291A>T	NP_000369.4:p.Arg431Trp
NM_024424.4:c.1342A>T	NP_077742.3:p.Arg448Trp
NM_024426.5:c.1342A>T	NP_077744.4:p.Arg448Trp
NM_001367854.1:c.154A>T	NP_001354783.1:p.Arg52Trp
NR_160306.1:n.1674A>T
NM_000378.6:c.1291A>T	NP_000369.4:p.Arg431Trp
NM_001198552.2:c.640A>T	NP_001185481.1:p.Arg214Trp
NM_024424.5:c.1342A>T	NP_077742.3:p.Arg448Trp
NM_024426.6:c.1342A>T MANE Select	NP_077744.4:p.Arg448Trp