Canonical Allele Identifier: CA379958719

Gene: WT1

Linked Data

• dbSNP Id: rs2132913768
• MyVariant Identifiers: chr11:g.32413533G>C (hg19) ; chr11:g.32391987G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391987G>C , CM000673.2:g.32391987G>C	GRCh38
NC_000011.9:g.32413533G>C , CM000673.1:g.32413533G>C	GRCh37
NC_000011.8:g.32370109G>C	NCBI36
NG_009272.1:g.48555C>G , LRG_525:g.48555C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1381C>G	ENSP00000331327.5:p.His461Asp
ENST00000379077.9:c.*616C>G	ENSP00000368368.5:n.*616C>G
ENST00000379079.8:c.781C>G	ENSP00000368370.2:p.His261Asp
ENST00000448076.9:c.1432C>G	ENSP00000413452.5:p.His478Asp
ENST00000452863.10:c.1432C>G MANE Select	ENSP00000415516.5:p.His478Asp
ENST00000526685.2:n.886C>G
ENST00000639563.3:c.1381C>G	ENSP00000492269.3:p.His461Asp
ENST00000639907.2:n.575C>G
ENST00000640146.2:c.757C>G	ENSP00000491984.2:p.His253Asp
ENST00000650745.1:n.1242C>G
ENST00000650861.1:n.2013C>G
ENST00000650986.1:n.95C>G
ENST00000651459.1:c.203C>G
ENST00000651533.1:n.478C>G
ENST00000651668.1:n.369C>G
ENST00000651794.1:n.1275C>G
ENST00000651819.1:n.357C>G
ENST00000652579.1:n.692C>G
ENST00000652724.1:n.622C>G
ENST00000332351.7:c.1417C>G	ENSP00000331327.3:p.His473Asp
ENST00000379077.7:c.*616C>G	ENSP00000368368.3:n.*616C>G
ENST00000379079.6:c.781C>G	ENSP00000368370.2:p.His261Asp
ENST00000448076.7:c.1417C>G	ENSP00000413452.3:p.His473Asp
ENST00000452863.7:c.1366C>G	ENSP00000415516.3:p.His456Asp
ENST00000527882.5:c.398C>G
ENST00000530998.5:c.730C>G	ENSP00000435307.1:p.His244Asp
NM_000378.4:c.1366C>G	NP_000369.3:p.His456Asp
NM_001198551.1:c.781C>G , LRG_525t2:c.781C>G	NP_001185480.1:p.His261Asp
NM_001198552.1:c.730C>G	NP_001185481.1:p.His244Asp
NM_024424.3:c.1417C>G	NP_077742.2:p.His473Asp
NM_024426.4:c.1417C>G	NP_077744.3:p.His473Asp
NM_000378.5:c.1381C>G	NP_000369.4:p.His461Asp
NM_024424.4:c.1432C>G	NP_077742.3:p.His478Asp
NM_024426.5:c.1432C>G	NP_077744.4:p.His478Asp
NM_001367854.1:c.244C>G	NP_001354783.1:p.His82Asp
NR_160306.1:n.1764C>G
NM_000378.6:c.1381C>G	NP_000369.4:p.His461Asp
NM_001198552.2:c.730C>G	NP_001185481.1:p.His244Asp
NM_024424.5:c.1432C>G	NP_077742.3:p.His478Asp
NM_024426.6:c.1432C>G MANE Select	NP_077744.4:p.His478Asp