Canonical Allele Identifier: CA2436414828

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299848_71299853delinsTGAATG , CM000685.2:g.71299848_71299853delinsTGAATG	GRCh38
NC_000023.10:g.70519698_70519703delinsTGAATG , CM000685.1:g.70519698_70519703delinsTGAATG	GRCh37
NC_000023.9:g.70436423_70436428delinsTGAATG	NCBI36
NG_046742.1:g.21657_21662delinsTGAATG
NG_054891.1:g.3574_3579delinsTGAATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000276079.13:c.1282-94_1282-89delinsTGAATG MANE Select	ENSP00000276079.8:n.1282-94_1282-89delins...
ENST00000373856.8:c.1379+90_1380-89delinsTGAATG	ENSP00000362963.4:n.1379+90_1380-89delins...
ENST00000420903.6:c.1282-94_1282-89delinsTGAATG	ENSP00000410299.2:n.1282-94_1282-89delins...
ENST00000450092.6:c.1282-94_1282-89delinsTGAATG	ENSP00000415777.2:n.1282-94_1282-89delins...
ENST00000454976.2:c.1282-94_1282-89delinsTGAATG	ENSP00000406673.2:n.1282-94_1282-89delins...
ENST00000473525.2:n.1990-94_1990-89delinsTGAATG
ENST00000676495.1:n.2693-94_2693-89delinsTGAATG
ENST00000676499.1:n.2238-94_2238-89delinsTGAATG
ENST00000676797.1:c.1015-94_1015-89delinsTGAATG	ENSP00000503920.1:n.1015-94_1015-89delins...
ENST00000677014.1:c.*1109-94_*1109-89delinsTGAATG	ENSP00000503813.1:n.*1109-94_*1109-89deli...
ENST00000677218.1:n.2453-94_2453-89delinsTGAATG
ENST00000677245.1:c.*1491-94_*1491-89delinsTGAATG	ENSP00000503929.1:n.*1491-94_*1491-89deli...
ENST00000677274.1:c.1282-94_1282-89delinsTGAATG	ENSP00000504314.1:n.1282-94_1282-89delins...
ENST00000677446.1:c.1282-94_1282-89delinsTGAATG	ENSP00000503031.1:n.1282-94_1282-89delins...
ENST00000677612.1:c.1282-94_1282-89delinsTGAATG	ENSP00000504351.1:n.1282-94_1282-89delins...
ENST00000677766.1:n.3593_3598delinsTGAATG
ENST00000677826.1:n.2024-94_2024-89delinsTGAATG
ENST00000677879.1:c.1102-94_1102-89delinsTGAATG	ENSP00000504090.1:n.1102-94_1102-89delins...
ENST00000677977.1:n.3114-94_3114-89delinsTGAATG
ENST00000678231.1:c.1282-94_1282-89delinsTGAATG	ENSP00000503233.1:n.1282-94_1282-89delins...
ENST00000678323.1:n.2380-94_2380-89delinsTGAATG
ENST00000678335.1:c.*195-94_*195-89delinsTGAATG	ENSP00000503769.1:n.*195-94_*195-89delins...
ENST00000678437.1:c.1273-94_1273-89delinsTGAATG	ENSP00000504007.1:n.1273-94_1273-89delins...
ENST00000678660.1:c.1297-94_1297-89delinsTGAATG	ENSP00000504665.1:n.1297-94_1297-89delins...
ENST00000678830.1:c.1372-94_1372-89delinsTGAATG	ENSP00000504263.1:n.1372-94_1372-89delins...
ENST00000679029.1:c.*96-94_*96-89delinsTGAATG	ENSP00000504193.1:n.*96-94_*96-89delinsTG...
ENST00000679267.1:n.3395_3400delinsTGAATG
ENST00000276079.12:c.1282-94_1282-89delinsTGAATG	ENSP00000276079.8:n.1282-94_1282-89delins...
ENST00000373841.5:c.1282-94_1282-89delinsTGAATG	ENSP00000362947.1:n.1282-94_1282-89delins...
ENST00000373856.7:c.1282-94_1282-89delinsTGAATG	ENSP00000362963.3:n.1282-94_1282-89delins...
ENST00000472185.1:n.61-671_61-666delinsTGAATG
ENST00000473525.1:n.1056-94_1056-89delinsTGAATG
ENST00000474431.5:n.317-94_317-89delinsTGAATG
ENST00000490044.5:n.1989-94_1989-89delinsTGAATG
ENST00000535149.5:c.1015-94_1015-89delinsTGAATG	ENSP00000441364.1:n.1015-94_1015-89delins...
NM_001145408.1:c.1282-94_1282-89delinsTGAATG	NP_001138880.1:n.1282-94_1282-89delinsTGA...
NM_001145409.1:c.1282-94_1282-89delinsTGAATG	NP_001138881.1:n.1282-94_1282-89delinsTGA...
NM_001145410.1:c.1015-94_1015-89delinsTGAATG	NP_001138882.1:n.1015-94_1015-89delinsTGA...
NM_007363.4:c.1282-94_1282-89delinsTGAATG	NP_031389.3:n.1282-94_1282-89delinsTGAATG...
NM_007363.5:c.1282-94_1282-89delinsTGAATG MANE Select	NP_031389.3:n.1282-94_1282-89delinsTGAATG...
NM_001145408.2:c.1282-94_1282-89delinsTGAATG	NP_001138880.1:n.1282-94_1282-89delinsTGA...
NM_001145409.2:c.1282-94_1282-89delinsTGAATG	NP_001138881.1:n.1282-94_1282-89delinsTGA...
NM_001145410.2:c.1015-94_1015-89delinsTGAATG	NP_001138882.1:n.1015-94_1015-89delinsTGA...