Canonical Allele Identifier: CA2697553172

Gene: NONO

Linked Data

• ClinVar Variation Id: 2744096
• ClinVar RCV Id: RCV003560676

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299933_71299938del , CM000685.2:g.71299933_71299938del	GRCh38
NC_000023.10:g.70519783_70519788del , CM000685.1:g.70519783_70519788del	GRCh37
NC_000023.9:g.70436508_70436513del	NCBI36
NG_046742.1:g.21742_21747del
NG_054891.1:g.3659_3664del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1282-9_1282-4del MANE Select	ENSP00000276079.8:n.1282-9_1282-4del
ENST00000373856.8:c.1380-9_1380-4del	ENSP00000362963.4:n.1380-9_1380-4del
ENST00000420903.6:c.1282-9_1282-4del	ENSP00000410299.2:n.1282-9_1282-4del
ENST00000450092.6:c.1282-9_1282-4del	ENSP00000415777.2:n.1282-9_1282-4del
ENST00000454976.2:c.1282-9_1282-4del	ENSP00000406673.2:n.1282-9_1282-4del
ENST00000473525.2:n.1990-9_1990-4del
ENST00000676495.1:n.2693-9_2693-4del
ENST00000676499.1:n.2238-9_2238-4del
ENST00000676797.1:c.1015-9_1015-4del	ENSP00000503920.1:n.1015-9_1015-4del
ENST00000677014.1:c.*1109-9_*1109-4del	ENSP00000503813.1:n.*1109-9_*1109-4del
ENST00000677218.1:n.2453-9_2453-4del
ENST00000677245.1:c.*1491-9_*1491-4del	ENSP00000503929.1:n.*1491-9_*1491-4del
ENST00000677274.1:c.1282-9_1282-4del	ENSP00000504314.1:n.1282-9_1282-4del
ENST00000677446.1:c.1282-9_1282-4del	ENSP00000503031.1:n.1282-9_1282-4del
ENST00000677612.1:c.1282-9_1282-4del	ENSP00000504351.1:n.1282-9_1282-4del
ENST00000677766.1:n.3678_3683del
ENST00000677826.1:n.2024-9_2024-4del
ENST00000677879.1:c.1102-9_1102-4del	ENSP00000504090.1:n.1102-9_1102-4del
ENST00000677977.1:n.3114-9_3114-4del
ENST00000678231.1:c.1282-9_1282-4del	ENSP00000503233.1:n.1282-9_1282-4del
ENST00000678323.1:n.2380-9_2380-4del
ENST00000678335.1:c.*195-9_*195-4del	ENSP00000503769.1:n.*195-9_*195-4del
ENST00000678437.1:c.1273-9_1273-4del	ENSP00000504007.1:n.1273-9_1273-4del
ENST00000678660.1:c.1297-9_1297-4del	ENSP00000504665.1:n.1297-9_1297-4del
ENST00000678830.1:c.1372-9_1372-4del	ENSP00000504263.1:n.1372-9_1372-4del
ENST00000679029.1:c.*96-9_*96-4del	ENSP00000504193.1:n.*96-9_*96-4del
ENST00000679267.1:n.3480_3485del
ENST00000276079.12:c.1282-9_1282-4del	ENSP00000276079.8:n.1282-9_1282-4del
ENST00000373841.5:c.1282-9_1282-4del	ENSP00000362947.1:n.1282-9_1282-4del
ENST00000373856.7:c.1282-9_1282-4del	ENSP00000362963.3:n.1282-9_1282-4del
ENST00000472185.1:n.61-586_61-581del
ENST00000473525.1:n.1056-9_1056-4del
ENST00000474431.5:n.317-9_317-4del
ENST00000490044.5:n.1989-9_1989-4del
ENST00000535149.5:c.1015-9_1015-4del	ENSP00000441364.1:n.1015-9_1015-4del
NM_001145408.1:c.1282-9_1282-4del	NP_001138880.1:n.1282-9_1282-4del
NM_001145409.1:c.1282-9_1282-4del	NP_001138881.1:n.1282-9_1282-4del
NM_001145410.1:c.1015-9_1015-4del	NP_001138882.1:n.1015-9_1015-4del
NM_007363.4:c.1282-9_1282-4del	NP_031389.3:n.1282-9_1282-4del
NM_007363.5:c.1282-9_1282-4del MANE Select	NP_031389.3:n.1282-9_1282-4del
NM_001145408.2:c.1282-9_1282-4del	NP_001138880.1:n.1282-9_1282-4del
NM_001145409.2:c.1282-9_1282-4del	NP_001138881.1:n.1282-9_1282-4del
NM_001145410.2:c.1015-9_1015-4del	NP_001138882.1:n.1015-9_1015-4del