Canonical Allele Identifier: CA2579961811

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32416528_32416529delinsGG , CM000673.2:g.32416528_32416529delinsGG	GRCh38
NC_000011.9:g.32438074_32438075delinsGG , CM000673.1:g.32438074_32438075delinsGG	GRCh37
NC_000011.8:g.32394650_32394651delinsGG	NCBI36
NG_009272.1:g.24013_24014delinsCC , LRG_525:g.24013_24014delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.965+1048_965+1049delinsCC	ENSP00000331327.5:n.965+1048_965+1049delinsCC
ENST00000379077.9:c.*161_*162delinsCC	ENSP00000368368.5:n.*161_*162delinsCC
ENST00000379079.8:c.326_327delinsCC	ENSP00000368370.2:p.Gly109Ala
ENST00000448076.9:c.977_978delinsCC	ENSP00000413452.5:p.Gly326Ala
ENST00000452863.10:c.977_978delinsCC MANE Select	ENSP00000415516.5:p.Gly326Ala
ENST00000639563.3:c.965+1048_965+1049delinsCC	ENSP00000492269.3:n.965+1048_965+1049delinsCC
ENST00000640146.2:c.341+1048_341+1049delinsCC	ENSP00000491984.2:n.341+1048_341+1049delinsCC
ENST00000651794.1:n.720_721delinsCC
ENST00000332351.7:c.962_963delinsCC	ENSP00000331327.3:p.Gly321Ala
ENST00000379077.7:c.*161_*162delinsCC	ENSP00000368368.3:n.*161_*162delinsCC
ENST00000379079.6:c.326_327delinsCC	ENSP00000368370.2:p.Gly109Ala
ENST00000448076.7:c.962_963delinsCC	ENSP00000413452.3:p.Gly321Ala
ENST00000452863.7:c.950+1048_950+1049delinsCC	ENSP00000415516.3:n.950+1048_950+1049delinsCC
ENST00000527775.1:c.215_216delinsCC	ENSP00000435351.1:p.Gly72Ala
ENST00000527882.5:c.33_34delinsCC
ENST00000530998.5:c.314+1048_314+1049delinsCC	ENSP00000435307.1:n.314+1048_314+1049delinsCC
NM_000378.4:c.950+1048_950+1049delinsCC	NP_000369.3:n.950+1048_950+1049delinsCC
NM_001198551.1:c.326_327delinsCC , LRG_525t2:c.326_327delinsCC	NP_001185480.1:p.Gly109Ala
NM_001198552.1:c.314+1048_314+1049delinsCC	NP_001185481.1:n.314+1048_314+1049delinsCC
NM_024424.3:c.962_963delinsCC	NP_077742.2:p.Gly321Ala
NM_024426.4:c.962_963delinsCC	NP_077744.3:p.Gly321Ala
NM_000378.5:c.965+1048_965+1049delinsCC	NP_000369.4:n.965+1048_965+1049delinsCC
NM_024424.4:c.977_978delinsCC	NP_077742.3:p.Gly326Ala
NM_024426.5:c.977_978delinsCC	NP_077744.4:p.Gly326Ala
NR_160306.1:n.1309_1310delinsCC
NM_000378.6:c.965+1048_965+1049delinsCC	NP_000369.4:n.965+1048_965+1049delinsCC
NM_001198552.2:c.314+1048_314+1049delinsCC	NP_001185481.1:n.314+1048_314+1049delinsCC
NM_024424.5:c.977_978delinsCC	NP_077742.3:p.Gly326Ala
NM_024426.6:c.977_978delinsCC MANE Select	NP_077744.4:p.Gly326Ala