Canonical Allele Identifier: CA379958807

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392008G>T , CM000673.2:g.32392008G>T	GRCh38
NC_000011.9:g.32413554G>T , CM000673.1:g.32413554G>T	GRCh37
NC_000011.8:g.32370130G>T	NCBI36
NG_009272.1:g.48534C>A , LRG_525:g.48534C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024426.6:c.1411C>A MANE Select	NP_077744.4:p.Leu471Met
ENST00000452863.10:c.1411C>A MANE Select	ENSP00000415516.5:p.Leu471Met
NM_000378.4:c.1345C>A	NP_000369.3:p.Leu449Met
NM_000378.5:c.1360C>A	NP_000369.4:p.Leu454Met
NM_000378.6:c.1360C>A	NP_000369.4:p.Leu454Met
NM_001198551.1:c.760C>A , LRG_525t2:c.760C>A	NP_001185480.1:p.Leu254Met
NM_001198552.1:c.709C>A	NP_001185481.1:p.Leu237Met
NM_001198552.2:c.709C>A	NP_001185481.1:p.Leu237Met
NM_001367854.1:c.223C>A	NP_001354783.1:p.Leu75Met
NM_024424.3:c.1396C>A	NP_077742.2:p.Leu466Met
NM_024424.4:c.1411C>A	NP_077742.3:p.Leu471Met
NM_024424.5:c.1411C>A	NP_077742.3:p.Leu471Met
NM_024426.4:c.1396C>A	NP_077744.3:p.Leu466Met
NM_024426.5:c.1411C>A	NP_077744.4:p.Leu471Met
NR_160306.1:n.1743C>A
ENST00000332351.7:c.1396C>A	ENSP00000331327.3:p.Leu466Met
ENST00000332351.9:c.1360C>A	ENSP00000331327.5:p.Leu454Met
ENST00000379077.7:c.*595C>A	ENSP00000368368.3:n.*595C>A
ENST00000379077.9:c.*595C>A	ENSP00000368368.5:n.*595C>A
ENST00000379079.6:c.760C>A	ENSP00000368370.2:p.Leu254Met
ENST00000379079.8:c.760C>A	ENSP00000368370.2:p.Leu254Met
ENST00000448076.7:c.1396C>A	ENSP00000413452.3:p.Leu466Met
ENST00000448076.9:c.1411C>A	ENSP00000413452.5:p.Leu471Met
ENST00000452863.7:c.1345C>A	ENSP00000415516.3:p.Leu449Met
ENST00000526685.2:n.865C>A
ENST00000527882.5:c.377C>A
ENST00000530998.5:c.709C>A	ENSP00000435307.1:p.Leu237Met
ENST00000639563.3:c.1360C>A	ENSP00000492269.3:p.Leu454Met
ENST00000639907.2:n.554C>A
ENST00000640146.2:c.736C>A	ENSP00000491984.2:p.Leu246Met
ENST00000650745.1:n.1221C>A
ENST00000650861.1:n.1992C>A
ENST00000650986.1:n.74C>A
ENST00000651459.1:c.182C>A
ENST00000651533.1:n.457C>A
ENST00000651668.1:n.348C>A
ENST00000651794.1:n.1254C>A
ENST00000651819.1:n.336C>A
ENST00000652579.1:n.671C>A
ENST00000652724.1:n.601C>A