Canonical Allele Identifier: CA379957559

Gene: WT1

Linked Data

• dbSNP Id: rs1451629862
• MyVariant Identifiers: chr11:g.32410649G>C (hg19) ; chr11:g.32389103G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32389103G>C , CM000673.2:g.32389103G>C	GRCh38
NC_000011.9:g.32410649G>C , CM000673.1:g.32410649G>C	GRCh37
NC_000011.8:g.32367225G>C	NCBI36
NG_009272.1:g.51439C>G , LRG_525:g.51439C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1464C>G	ENSP00000331327.5:p.His488Gln
ENST00000379077.9:c.*708C>G	ENSP00000368368.5:n.*708C>G
ENST00000379079.8:c.864C>G	ENSP00000368370.2:p.His288Gln
ENST00000448076.9:c.1515C>G	ENSP00000413452.5:p.His505Gln
ENST00000452863.10:c.1524C>G MANE Select	ENSP00000415516.5:p.His508Gln
ENST00000526685.2:n.969C>G
ENST00000639563.3:c.1473C>G	ENSP00000492269.3:p.His491Gln
ENST00000639907.2:n.658C>G
ENST00000640146.2:c.849C>G	ENSP00000491984.2:p.His283Gln
ENST00000650745.1:n.1334C>G
ENST00000650861.1:n.2096C>G
ENST00000650986.1:n.187C>G
ENST00000651459.1:c.295C>G
ENST00000651533.1:n.561C>G
ENST00000651668.1:n.461C>G
ENST00000651794.1:n.1367C>G
ENST00000651819.1:n.449C>G
ENST00000652579.1:n.784C>G
ENST00000652724.1:n.714C>G
ENST00000332351.7:c.1509C>G	ENSP00000331327.3:p.His503Gln
ENST00000379077.7:c.*708C>G	ENSP00000368368.3:n.*708C>G
ENST00000379079.6:c.864C>G	ENSP00000368370.2:p.His288Gln
ENST00000448076.7:c.1500C>G	ENSP00000413452.3:p.His500Gln
ENST00000452863.7:c.1449C>G	ENSP00000415516.3:p.His483Gln
ENST00000527882.5:c.490C>G
ENST00000530998.5:c.822C>G	ENSP00000435307.1:p.His274Gln
NM_000378.4:c.1449C>G	NP_000369.3:p.His483Gln
NM_001198551.1:c.864C>G , LRG_525t2:c.864C>G	NP_001185480.1:p.His288Gln
NM_001198552.1:c.822C>G	NP_001185481.1:p.His274Gln
NM_024424.3:c.1500C>G	NP_077742.2:p.His500Gln
NM_024426.4:c.1509C>G	NP_077744.3:p.His503Gln
NM_000378.5:c.1464C>G	NP_000369.4:p.His488Gln
NM_024424.4:c.1515C>G	NP_077742.3:p.His505Gln
NM_024426.5:c.1524C>G	NP_077744.4:p.His508Gln
NM_001367854.1:c.336C>G	NP_001354783.1:p.His112Gln
NR_160306.1:n.1856C>G
NM_000378.6:c.1464C>G	NP_000369.4:p.His488Gln
NM_001198552.2:c.822C>G	NP_001185481.1:p.His274Gln
NM_024424.5:c.1515C>G	NP_077742.3:p.His505Gln
NM_024426.6:c.1524C>G MANE Select	NP_077744.4:p.His508Gln