Canonical Allele Identifier: CA2436414844

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299922_71299924delinsGCT , CM000685.2:g.71299922_71299924delinsGCT	GRCh38
NC_000023.10:g.70519772_70519774delinsGCT , CM000685.1:g.70519772_70519774delinsGCT	GRCh37
NC_000023.9:g.70436497_70436499delinsGCT	NCBI36
NG_046742.1:g.21731_21733delinsGCT
NG_054891.1:g.3648_3650delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1282-20_1282-18delinsGCT MANE Select	ENSP00000276079.8:n.1282-20_1282-18delinsGCT
ENST00000373856.8:c.1380-20_1380-18delinsGCT	ENSP00000362963.4:n.1380-20_1380-18delinsGCT
ENST00000420903.6:c.1282-20_1282-18delinsGCT	ENSP00000410299.2:n.1282-20_1282-18delinsGCT
ENST00000450092.6:c.1282-20_1282-18delinsGCT	ENSP00000415777.2:n.1282-20_1282-18delinsGCT
ENST00000454976.2:c.1282-20_1282-18delinsGCT	ENSP00000406673.2:n.1282-20_1282-18delinsGCT
ENST00000473525.2:n.1990-20_1990-18delinsGCT
ENST00000676495.1:n.2693-20_2693-18delinsGCT
ENST00000676499.1:n.2238-20_2238-18delinsGCT
ENST00000676797.1:c.1015-20_1015-18delinsGCT	ENSP00000503920.1:n.1015-20_1015-18delinsGCT
ENST00000677014.1:c.*1109-20_*1109-18delinsGCT	ENSP00000503813.1:n.*1109-20_*1109-18delinsGCT
ENST00000677218.1:n.2453-20_2453-18delinsGCT
ENST00000677245.1:c.*1491-20_*1491-18delinsGCT	ENSP00000503929.1:n.*1491-20_*1491-18delinsGCT
ENST00000677274.1:c.1282-20_1282-18delinsGCT	ENSP00000504314.1:n.1282-20_1282-18delinsGCT
ENST00000677446.1:c.1282-20_1282-18delinsGCT	ENSP00000503031.1:n.1282-20_1282-18delinsGCT
ENST00000677612.1:c.1282-20_1282-18delinsGCT	ENSP00000504351.1:n.1282-20_1282-18delinsGCT
ENST00000677766.1:n.3667_3669delinsGCT
ENST00000677826.1:n.2024-20_2024-18delinsGCT
ENST00000677879.1:c.1102-20_1102-18delinsGCT	ENSP00000504090.1:n.1102-20_1102-18delinsGCT
ENST00000677977.1:n.3114-20_3114-18delinsGCT
ENST00000678231.1:c.1282-20_1282-18delinsGCT	ENSP00000503233.1:n.1282-20_1282-18delinsGCT
ENST00000678323.1:n.2380-20_2380-18delinsGCT
ENST00000678335.1:c.*195-20_*195-18delinsGCT	ENSP00000503769.1:n.*195-20_*195-18delinsGCT
ENST00000678437.1:c.1273-20_1273-18delinsGCT	ENSP00000504007.1:n.1273-20_1273-18delinsGCT
ENST00000678660.1:c.1297-20_1297-18delinsGCT	ENSP00000504665.1:n.1297-20_1297-18delinsGCT
ENST00000678830.1:c.1372-20_1372-18delinsGCT	ENSP00000504263.1:n.1372-20_1372-18delinsGCT
ENST00000679029.1:c.*96-20_*96-18delinsGCT	ENSP00000504193.1:n.*96-20_*96-18delinsGCT
ENST00000679267.1:n.3469_3471delinsGCT
ENST00000276079.12:c.1282-20_1282-18delinsGCT	ENSP00000276079.8:n.1282-20_1282-18delinsGCT
ENST00000373841.5:c.1282-20_1282-18delinsGCT	ENSP00000362947.1:n.1282-20_1282-18delinsGCT
ENST00000373856.7:c.1282-20_1282-18delinsGCT	ENSP00000362963.3:n.1282-20_1282-18delinsGCT
ENST00000472185.1:n.61-597_61-595delinsGCT
ENST00000473525.1:n.1056-20_1056-18delinsGCT
ENST00000474431.5:n.317-20_317-18delinsGCT
ENST00000490044.5:n.1989-20_1989-18delinsGCT
ENST00000535149.5:c.1015-20_1015-18delinsGCT	ENSP00000441364.1:n.1015-20_1015-18delinsGCT
NM_001145408.1:c.1282-20_1282-18delinsGCT	NP_001138880.1:n.1282-20_1282-18delinsGCT
NM_001145409.1:c.1282-20_1282-18delinsGCT	NP_001138881.1:n.1282-20_1282-18delinsGCT
NM_001145410.1:c.1015-20_1015-18delinsGCT	NP_001138882.1:n.1015-20_1015-18delinsGCT
NM_007363.4:c.1282-20_1282-18delinsGCT	NP_031389.3:n.1282-20_1282-18delinsGCT
NM_007363.5:c.1282-20_1282-18delinsGCT MANE Select	NP_031389.3:n.1282-20_1282-18delinsGCT
NM_001145408.2:c.1282-20_1282-18delinsGCT	NP_001138880.1:n.1282-20_1282-18delinsGCT
NM_001145409.2:c.1282-20_1282-18delinsGCT	NP_001138881.1:n.1282-20_1282-18delinsGCT
NM_001145410.2:c.1015-20_1015-18delinsGCT	NP_001138882.1:n.1015-20_1015-18delinsGCT