Canonical Allele Identifier: CA2579961856

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32416533_32416534delinsTG , CM000673.2:g.32416533_32416534delinsTG	GRCh38
NC_000011.9:g.32438079_32438080delinsTG , CM000673.1:g.32438079_32438080delinsTG	GRCh37
NC_000011.8:g.32394655_32394656delinsTG	NCBI36
NG_009272.1:g.24008_24009delinsCA , LRG_525:g.24008_24009delinsCA

Transcript Alleles

HGVS	Amino-acid Change
NM_024426.6:c.972_973delinsCA MANE Select	NP_077744.4:p.Ala325Thr
ENST00000452863.10:c.972_973delinsCA MANE Select	ENSP00000415516.5:p.Ala325Thr
NM_000378.4:c.950+1043_950+1044delinsCA	NP_000369.3:n.950+1043_950+1044delinsCA
NM_000378.5:c.965+1043_965+1044delinsCA	NP_000369.4:n.965+1043_965+1044delinsCA
NM_000378.6:c.965+1043_965+1044delinsCA	NP_000369.4:n.965+1043_965+1044delinsCA
NM_001198551.1:c.321_322delinsCA , LRG_525t2:c.321_322delinsCA	NP_001185480.1:p.Ala108Thr
NM_001198552.1:c.314+1043_314+1044delinsCA	NP_001185481.1:n.314+1043_314+1044delinsCA
NM_001198552.2:c.314+1043_314+1044delinsCA	NP_001185481.1:n.314+1043_314+1044delinsCA
NM_024424.3:c.957_958delinsCA	NP_077742.2:p.Ala320Thr
NM_024424.4:c.972_973delinsCA	NP_077742.3:p.Ala325Thr
NM_024424.5:c.972_973delinsCA	NP_077742.3:p.Ala325Thr
NM_024426.4:c.957_958delinsCA	NP_077744.3:p.Ala320Thr
NM_024426.5:c.972_973delinsCA	NP_077744.4:p.Ala325Thr
NR_160306.1:n.1304_1305delinsCA
ENST00000332351.7:c.957_958delinsCA	ENSP00000331327.3:p.Ala320Thr
ENST00000332351.9:c.965+1043_965+1044delinsCA	ENSP00000331327.5:n.965+1043_965+1044delinsCA
ENST00000379077.7:c.*156_*157delinsCA	ENSP00000368368.3:n.*156_*157delinsCA
ENST00000379077.9:c.*156_*157delinsCA	ENSP00000368368.5:n.*156_*157delinsCA
ENST00000379079.6:c.321_322delinsCA	ENSP00000368370.2:p.Ala108Thr
ENST00000379079.8:c.321_322delinsCA	ENSP00000368370.2:p.Ala108Thr
ENST00000448076.7:c.957_958delinsCA	ENSP00000413452.3:p.Ala320Thr
ENST00000448076.9:c.972_973delinsCA	ENSP00000413452.5:p.Ala325Thr
ENST00000452863.7:c.950+1043_950+1044delinsCA	ENSP00000415516.3:n.950+1043_950+1044delinsCA
ENST00000527775.1:c.210_211delinsCA	ENSP00000435351.1:p.Ala71Thr
ENST00000527882.5:c.28_29delinsCA
ENST00000530998.5:c.314+1043_314+1044delinsCA	ENSP00000435307.1:n.314+1043_314+1044delinsCA
ENST00000639563.3:c.965+1043_965+1044delinsCA	ENSP00000492269.3:n.965+1043_965+1044delinsCA
ENST00000640146.2:c.341+1043_341+1044delinsCA	ENSP00000491984.2:n.341+1043_341+1044delinsCA
ENST00000651794.1:n.715_716delinsCA