Canonical Allele Identifier: CA379959198

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32414238A>C (hg19) ; chr11:g.32392692A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392692A>C , CM000673.2:g.32392692A>C	GRCh38
NC_000011.9:g.32414238A>C , CM000673.1:g.32414238A>C	GRCh37
NC_000011.8:g.32370814A>C	NCBI36
NG_009272.1:g.47850T>G , LRG_525:g.47850T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1277T>G	ENSP00000331327.5:p.Leu426Arg
ENST00000379077.9:c.*512T>G	ENSP00000368368.5:n.*512T>G
ENST00000379079.8:c.677T>G	ENSP00000368370.2:p.Leu226Arg
ENST00000448076.9:c.1328T>G	ENSP00000413452.5:p.Leu443Arg
ENST00000452863.10:c.1328T>G MANE Select	ENSP00000415516.5:p.Leu443Arg
ENST00000526685.2:n.782T>G
ENST00000639563.3:c.1277T>G	ENSP00000492269.3:p.Leu426Arg
ENST00000639907.2:n.471T>G
ENST00000640146.2:c.653T>G	ENSP00000491984.2:p.Leu218Arg
ENST00000650745.1:n.537T>G
ENST00000650861.1:n.1909T>G
ENST00000651459.1:c.99T>G
ENST00000651533.1:n.374T>G
ENST00000651668.1:n.265T>G
ENST00000651794.1:n.1171T>G
ENST00000651819.1:n.253T>G
ENST00000652579.1:n.588T>G
ENST00000652724.1:n.518T>G
ENST00000332351.7:c.1313T>G	ENSP00000331327.3:p.Leu438Arg
ENST00000379077.7:c.*512T>G	ENSP00000368368.3:n.*512T>G
ENST00000379079.6:c.677T>G	ENSP00000368370.2:p.Leu226Arg
ENST00000448076.7:c.1313T>G	ENSP00000413452.3:p.Leu438Arg
ENST00000452863.7:c.1262T>G	ENSP00000415516.3:p.Leu421Arg
ENST00000527882.5:c.321-628T>G
ENST00000530998.5:c.626T>G	ENSP00000435307.1:p.Leu209Arg
NM_000378.4:c.1262T>G	NP_000369.3:p.Leu421Arg
NM_001198551.1:c.677T>G , LRG_525t2:c.677T>G	NP_001185480.1:p.Leu226Arg
NM_001198552.1:c.626T>G	NP_001185481.1:p.Leu209Arg
NM_024424.3:c.1313T>G	NP_077742.2:p.Leu438Arg
NM_024426.4:c.1313T>G	NP_077744.3:p.Leu438Arg
NM_000378.5:c.1277T>G	NP_000369.4:p.Leu426Arg
NM_024424.4:c.1328T>G	NP_077742.3:p.Leu443Arg
NM_024426.5:c.1328T>G	NP_077744.4:p.Leu443Arg
NM_001367854.1:c.140T>G	NP_001354783.1:p.Leu47Arg
NR_160306.1:n.1660T>G
NM_000378.6:c.1277T>G	NP_000369.4:p.Leu426Arg
NM_001198552.2:c.626T>G	NP_001185481.1:p.Leu209Arg
NM_024424.5:c.1328T>G	NP_077742.3:p.Leu443Arg
NM_024426.6:c.1328T>G MANE Select	NP_077744.4:p.Leu443Arg