Canonical Allele Identifier: CA379958668

Gene: WT1

Linked Data

• MyVariant Identifiers: chr11:g.32413523T>C (hg19) ; chr11:g.32391977T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32391977T>C , CM000673.2:g.32391977T>C	GRCh38
NC_000011.9:g.32413523T>C , CM000673.1:g.32413523T>C	GRCh37
NC_000011.8:g.32370099T>C	NCBI36
NG_009272.1:g.48565A>G , LRG_525:g.48565A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1387+4A>G	ENSP00000331327.5:n.1387+4A>G
ENST00000379077.9:c.*626A>G	ENSP00000368368.5:n.*626A>G
ENST00000379079.8:c.787+4A>G	ENSP00000368370.2:n.787+4A>G
ENST00000448076.9:c.1438+4A>G	ENSP00000413452.5:n.1438+4A>G
ENST00000452863.10:c.1442A>G MANE Select	ENSP00000415516.5:p.Lys481Arg
ENST00000526685.2:n.892+4A>G
ENST00000639563.3:c.1391A>G	ENSP00000492269.3:p.Lys464Arg
ENST00000639907.2:n.581+4A>G
ENST00000640146.2:c.767A>G	ENSP00000491984.2:p.Lys256Arg
ENST00000650745.1:n.1252A>G
ENST00000650861.1:n.2019+4A>G
ENST00000650986.1:n.105A>G
ENST00000651459.1:c.213A>G
ENST00000651533.1:n.484+4A>G
ENST00000651668.1:n.379A>G
ENST00000651794.1:n.1285A>G
ENST00000651819.1:n.367A>G
ENST00000652579.1:n.702A>G
ENST00000652724.1:n.632A>G
ENST00000332351.7:c.1427A>G	ENSP00000331327.3:p.Lys476Arg
ENST00000379077.7:c.*626A>G	ENSP00000368368.3:n.*626A>G
ENST00000379079.6:c.787+4A>G	ENSP00000368370.2:n.787+4A>G
ENST00000448076.7:c.1423+4A>G	ENSP00000413452.3:n.1423+4A>G
ENST00000452863.7:c.1372+4A>G	ENSP00000415516.3:n.1372+4A>G
ENST00000527882.5:c.408A>G
ENST00000530998.5:c.740A>G	ENSP00000435307.1:p.Lys247Arg
NM_000378.4:c.1372+4A>G	NP_000369.3:n.1372+4A>G
NM_001198551.1:c.787+4A>G , LRG_525t2:c.787+4A>G	NP_001185480.1:n.787+4A>G
NM_001198552.1:c.740A>G	NP_001185481.1:p.Lys247Arg
NM_024424.3:c.1423+4A>G	NP_077742.2:n.1423+4A>G
NM_024426.4:c.1427A>G	NP_077744.3:p.Lys476Arg
NM_000378.5:c.1387+4A>G	NP_000369.4:n.1387+4A>G
NM_024424.4:c.1438+4A>G	NP_077742.3:n.1438+4A>G
NM_024426.5:c.1442A>G	NP_077744.4:p.Lys481Arg
NM_001367854.1:c.254A>G	NP_001354783.1:p.Lys85Arg
NR_160306.1:n.1774A>G
NM_000378.6:c.1387+4A>G	NP_000369.4:n.1387+4A>G
NM_001198552.2:c.740A>G	NP_001185481.1:p.Lys247Arg
NM_024424.5:c.1438+4A>G	NP_077742.3:n.1438+4A>G
NM_024426.6:c.1442A>G MANE Select	NP_077744.4:p.Lys481Arg