Canonical Allele Identifier: CA351658

Gene: NONO

Linked Data

• ClinVar Variation Id: 222082
• ClinVar RCV Id: RCV000207520
• dbSNP Id: rs869025344
• MyVariant Identifiers: chrX:g.70519904dupC (hg19) ; chrX:g.71300054dupC (hg38)
• PubMed: PMID:26571461 ; PMID:27550220

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300054dup , CM000685.2:g.71300054dup	GRCh38
NC_000023.10:g.70519904dup , CM000685.1:g.70519904dup	GRCh37
NC_000023.9:g.70436629dup	NCBI36
NG_046742.1:g.21863dup
NG_054891.1:g.3780dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1394dup MANE Select	ENSP00000276079.8:p.Asn466LysfsTer13
ENST00000373856.8:c.1492dup	ENSP00000362963.4:p.Gln498ProfsTer8
ENST00000420903.6:c.1394dup	ENSP00000410299.2:p.Asn466LysfsTer13
ENST00000450092.6:c.1394dup	ENSP00000415777.2:p.Asn466LysfsTer?
ENST00000454976.2:c.1394dup	ENSP00000406673.2:p.Asn466LysfsTer?
ENST00000473525.2:n.2102dup
ENST00000676495.1:n.2805dup
ENST00000676499.1:n.2350dup
ENST00000676797.1:c.1127dup	ENSP00000503920.1:p.Asn377LysfsTer13
ENST00000677014.1:c.*1221dup	ENSP00000503813.1:n.*1221dup
ENST00000677218.1:n.2565dup
ENST00000677245.1:c.*1603dup	ENSP00000503929.1:n.*1603dup
ENST00000677274.1:c.1394dup	ENSP00000504314.1:p.Asn466LysfsTer13
ENST00000677446.1:c.1394dup	ENSP00000503031.1:p.Asn466LysfsTer13
ENST00000677612.1:c.1394dup	ENSP00000504351.1:p.Asn466LysfsTer13
ENST00000677766.1:n.3799dup
ENST00000677826.1:n.2136dup
ENST00000677879.1:c.1214dup	ENSP00000504090.1:p.Asn406LysfsTer13
ENST00000677977.1:n.3226dup
ENST00000678231.1:c.1394dup	ENSP00000503233.1:p.Asn466LysfsTer13
ENST00000678323.1:n.2492dup
ENST00000678335.1:c.*307dup	ENSP00000503769.1:n.*307dup
ENST00000678437.1:c.1385dup	ENSP00000504007.1:p.Asn463LysfsTer13
ENST00000678660.1:c.1409dup	ENSP00000504665.1:p.Asn471LysfsTer13
ENST00000678830.1:c.1484dup	ENSP00000504263.1:p.Asn496LysfsTer13
ENST00000679029.1:c.*208dup	ENSP00000504193.1:n.*208dup
ENST00000679267.1:n.3601dup
ENST00000276079.12:c.1394dup	ENSP00000276079.8:p.Asn466LysfsTer13
ENST00000373841.5:c.1394dup	ENSP00000362947.1:p.Asn466LysfsTer13
ENST00000373856.7:c.1394dup	ENSP00000362963.3:p.Asn466LysfsTer13
ENST00000472185.1:n.61-465dup
ENST00000473525.1:n.1168dup
ENST00000474431.5:n.429dup
ENST00000490044.5:n.2101dup
ENST00000535149.5:c.1127dup	ENSP00000441364.1:p.Asn377LysfsTer13
NM_001145408.1:c.1394dup	NP_001138880.1:p.Asn466LysfsTer13
NM_001145409.1:c.1394dup	NP_001138881.1:p.Asn466LysfsTer13
NM_001145410.1:c.1127dup	NP_001138882.1:p.Asn377LysfsTer13
NM_007363.4:c.1394dup	NP_031389.3:p.Asn466LysfsTer13
NM_007363.5:c.1394dup MANE Select	NP_031389.3:p.Asn466LysfsTer13
NM_001145408.2:c.1394dup	NP_001138880.1:p.Asn466LysfsTer13
NM_001145409.2:c.1394dup	NP_001138881.1:p.Asn466LysfsTer13
NM_001145410.2:c.1127dup	NP_001138882.1:p.Asn377LysfsTer13