Canonical Allele Identifier: CA16043280
Gene: NONO HGNC NCBI

Linked Data

ClinVar Variation Id: 373550
ClinVar RCV Id: RCV000413763
dbSNP Id: rs1057518476

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71291854_71291855del , CM000685.2:g.71291854_71291855del GRCh38
NC_000023.10:g.70511704_70511705del , CM000685.1:g.70511704_70511705del GRCh37
NC_000023.9:g.70428429_70428430del NCBI36
NG_046742.1:g.13663_13664del

Transcript Alleles

HGVS Amino-acid change
ENST00000276079.13:c.230_231del MANE Select ENSP00000276079.8:p.Phe77CysfsTer10
ENST00000373856.8:c.230_231del ENSP00000362963.4:p.Phe77CysfsTer10
ENST00000420903.6:c.230_231del ENSP00000410299.2:p.Phe77CysfsTer10
ENST00000450092.6:c.230_231del ENSP00000415777.2:p.Phe77CysfsTer10
ENST00000454976.2:c.230_231del ENSP00000406673.2:p.Phe77CysfsTer10
ENST00000471419.7:n.1342_1343del
ENST00000473525.2:n.408_409del
ENST00000676495.1:n.408_409del
ENST00000676499.1:n.408_409del
ENST00000676797.1:c.-38_-37del ENSP00000503920.1:n.-38_-37del
ENST00000677014.1:c.*57_*58del ENSP00000503813.1:n.*57_*58del
ENST00000677218.1:n.497_498del
ENST00000677245.1:c.230_231del ENSP00000503929.1:p.Phe77CysfsTer10
ENST00000677274.1:c.230_231del ENSP00000504314.1:p.Phe77CysfsTer10
ENST00000677446.1:c.230_231del ENSP00000503031.1:p.Phe77CysfsTer10
ENST00000677612.1:c.230_231del ENSP00000504351.1:p.Phe77CysfsTer10
ENST00000677766.1:n.408_409del
ENST00000677826.1:n.408_409del
ENST00000677879.1:c.230_231del ENSP00000504090.1:p.Phe77CysfsTer10
ENST00000677977.1:n.1342_1343del
ENST00000678231.1:c.230_231del ENSP00000503233.1:p.Phe77CysfsTer10
ENST00000678323.1:n.408_409del
ENST00000678335.1:c.230_231del ENSP00000503769.1:p.Phe77CysfsTer10
ENST00000678437.1:c.230_231del ENSP00000504007.1:p.Phe77CysfsTer10
ENST00000678660.1:c.245_246del ENSP00000504665.1:p.Phe82CysfsTer10
ENST00000678830.1:c.230_231del ENSP00000504263.1:p.Phe77CysfsTer10
ENST00000679029.1:c.230_231del ENSP00000504193.1:p.Phe77CysfsTer10
ENST00000679062.1:n.1304_1305del
ENST00000679254.1:n.1392_1393del
ENST00000679267.1:n.408_409del
ENST00000276079.12:c.230_231del ENSP00000276079.8:p.Phe77CysfsTer10
ENST00000373841.5:c.230_231del ENSP00000362947.1:p.Phe77CysfsTer10
ENST00000373856.7:c.230_231del ENSP00000362963.3:p.Phe77CysfsTer10
ENST00000413858.5:c.230_231del ENSP00000413350.1:p.Phe77CysfsTer10
ENST00000420903.5:c.230_231del ENSP00000410299.1:p.Phe77CysfsTer10
ENST00000454976.1:c.230_231del ENSP00000406673.1:p.Phe77CysfsTer10
ENST00000472185.1:n.60+7448_60+7449del
ENST00000474431.5:n.71-5989_71-5988del
ENST00000486613.6:n.324_325del
ENST00000535149.5:c.-38_-37del ENSP00000441364.1:n.-38_-37del
NM_001145408.1:c.230_231del NP_001138880.1:p.Phe77CysfsTer10
NM_001145409.1:c.230_231del NP_001138881.1:p.Phe77CysfsTer10
NM_001145410.1:c.-38_-37del NP_001138882.1:n.-38_-37del
NM_007363.4:c.230_231del NP_031389.3:p.Phe77CysfsTer10
NM_007363.5:c.230_231del MANE Select NP_031389.3:p.Phe77CysfsTer10
NM_001145408.2:c.230_231del NP_001138880.1:p.Phe77CysfsTer10
NM_001145409.2:c.230_231del NP_001138881.1:p.Phe77CysfsTer10
NM_001145410.2:c.-38_-37del NP_001138882.1:n.-38_-37del