Canonical Allele Identifier: CA16621496
Gene: NONO HGNC NCBI

Linked Data

ClinVar Variation Id: 424120
ClinVar RCV Id: RCV000482877
dbSNP Id: rs1064796806

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71299949del , CM000685.2:g.71299949del GRCh38
NC_000023.10:g.70519799del , CM000685.1:g.70519799del GRCh37
NC_000023.9:g.70436524del NCBI36
NG_046742.1:g.21758del
NG_054891.1:g.3675del

Transcript Alleles

HGVS Amino-acid change
ENST00000276079.13:c.1289del MANE Select ENSP00000276079.8:p.Pro430GlnfsTer?
ENST00000373856.8:c.1387del ENSP00000362963.4:p.Gln463AsnfsTer3
ENST00000420903.6:c.1289del ENSP00000410299.2:p.Pro430GlnfsTer?
ENST00000450092.6:c.1289del ENSP00000415777.2:p.Pro430GlnfsTer?
ENST00000454976.2:c.1289del ENSP00000406673.2:p.Pro430GlnfsTer?
ENST00000473525.2:n.1997del
ENST00000676495.1:n.2700del
ENST00000676499.1:n.2245del
ENST00000676797.1:c.1022del ENSP00000503920.1:p.Pro341GlnfsTer?
ENST00000677014.1:c.*1116del ENSP00000503813.1:n.*1116del
ENST00000677218.1:n.2460del
ENST00000677245.1:c.*1498del ENSP00000503929.1:n.*1498del
ENST00000677274.1:c.1289del ENSP00000504314.1:p.Pro430GlnfsTer?
ENST00000677446.1:c.1289del ENSP00000503031.1:p.Pro430GlnfsTer?
ENST00000677612.1:c.1289del ENSP00000504351.1:p.Pro430GlnfsTer?
ENST00000677766.1:n.3694del
ENST00000677826.1:n.2031del
ENST00000677879.1:c.1109del ENSP00000504090.1:p.Pro370GlnfsTer?
ENST00000677977.1:n.3121del
ENST00000678231.1:c.1289del ENSP00000503233.1:p.Pro430GlnfsTer?
ENST00000678323.1:n.2387del
ENST00000678335.1:c.*202del ENSP00000503769.1:n.*202del
ENST00000678437.1:c.1280del ENSP00000504007.1:p.Pro427GlnfsTer?
ENST00000678660.1:c.1304del ENSP00000504665.1:p.Pro435GlnfsTer?
ENST00000678830.1:c.1379del ENSP00000504263.1:p.Pro460GlnfsTer?
ENST00000679029.1:c.*103del ENSP00000504193.1:n.*103del
ENST00000679267.1:n.3496del
ENST00000276079.12:c.1289del ENSP00000276079.8:p.Pro430GlnfsTer?
ENST00000373841.5:c.1289del ENSP00000362947.1:p.Pro430GlnfsTer?
ENST00000373856.7:c.1289del ENSP00000362963.3:p.Pro430GlnfsTer?
ENST00000472185.1:n.61-570del
ENST00000473525.1:n.1063del
ENST00000474431.5:n.324del
ENST00000490044.5:n.1996del
ENST00000535149.5:c.1022del ENSP00000441364.1:p.Pro341GlnfsTer?
NM_001145408.1:c.1289del NP_001138880.1:p.Pro430GlnfsTer?
NM_001145409.1:c.1289del NP_001138881.1:p.Pro430GlnfsTer?
NM_001145410.1:c.1022del NP_001138882.1:p.Pro341GlnfsTer?
NM_007363.4:c.1289del NP_031389.3:p.Pro430GlnfsTer?
NM_007363.5:c.1289del MANE Select NP_031389.3:p.Pro430GlnfsTer?
NM_001145408.2:c.1289del NP_001138880.1:p.Pro430GlnfsTer?
NM_001145409.2:c.1289del NP_001138881.1:p.Pro430GlnfsTer?
NM_001145410.2:c.1022del NP_001138882.1:p.Pro341GlnfsTer?