Canonical Allele Identifier: CA2436414809

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299793G= , CM000685.2:g.71299793G=	GRCh38
NC_000023.10:g.70519643G= , CM000685.1:g.70519643G=	GRCh37
NC_000023.9:g.70436368G=	NCBI36
NG_046742.1:g.21602G=
NG_054891.1:g.3519G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1282-149G= MANE Select	ENSP00000276079.8:n.1282-149G=
ENST00000373856.8:c.1379+35G=	ENSP00000362963.4:n.1379+35G=
ENST00000420903.6:c.1282-149G=	ENSP00000410299.2:n.1282-149G=
ENST00000450092.6:c.1282-149G=	ENSP00000415777.2:n.1282-149G=
ENST00000454976.2:c.1282-149G=	ENSP00000406673.2:n.1282-149G=
ENST00000473525.2:n.1990-149G=
ENST00000676495.1:n.2693-149G=
ENST00000676499.1:n.2238-149G=
ENST00000676797.1:c.1015-149G=	ENSP00000503920.1:n.1015-149G=
ENST00000677014.1:c.*1109-149G=	ENSP00000503813.1:n.*1109-149G=
ENST00000677218.1:n.2453-149G=
ENST00000677245.1:c.*1491-149G=	ENSP00000503929.1:n.*1491-149G=
ENST00000677274.1:c.1282-149G=	ENSP00000504314.1:n.1282-149G=
ENST00000677446.1:c.1282-149G=	ENSP00000503031.1:n.1282-149G=
ENST00000677612.1:c.1282-149G=	ENSP00000504351.1:n.1282-149G=
ENST00000677766.1:n.3538G=
ENST00000677826.1:n.2024-149G=
ENST00000677879.1:c.1102-149G=	ENSP00000504090.1:n.1102-149G=
ENST00000677977.1:n.3114-149G=
ENST00000678231.1:c.1282-149G=	ENSP00000503233.1:n.1282-149G=
ENST00000678323.1:n.2380-149G=
ENST00000678335.1:c.*195-149G=	ENSP00000503769.1:n.*195-149G=
ENST00000678437.1:c.1273-149G=	ENSP00000504007.1:n.1273-149G=
ENST00000678660.1:c.1297-149G=	ENSP00000504665.1:n.1297-149G=
ENST00000678830.1:c.1372-149G=	ENSP00000504263.1:n.1372-149G=
ENST00000679029.1:c.*96-149G=	ENSP00000504193.1:n.*96-149G=
ENST00000679267.1:n.3340G=
ENST00000276079.12:c.1282-149G=	ENSP00000276079.8:n.1282-149G=
ENST00000373841.5:c.1282-149G=	ENSP00000362947.1:n.1282-149G=
ENST00000373856.7:c.1282-149G=	ENSP00000362963.3:n.1282-149G=
ENST00000472185.1:n.61-726G=
ENST00000473525.1:n.1056-149G=
ENST00000474431.5:n.317-149G=
ENST00000490044.5:n.1989-149G=
ENST00000535149.5:c.1015-149G=	ENSP00000441364.1:n.1015-149G=
NM_001145408.1:c.1282-149G=	NP_001138880.1:n.1282-149G=
NM_001145409.1:c.1282-149G=	NP_001138881.1:n.1282-149G=
NM_001145410.1:c.1015-149G=	NP_001138882.1:n.1015-149G=
NM_007363.4:c.1282-149G=	NP_031389.3:n.1282-149G=
NM_007363.5:c.1282-149G= MANE Select	NP_031389.3:n.1282-149G=
NM_001145408.2:c.1282-149G=	NP_001138880.1:n.1282-149G=
NM_001145409.2:c.1282-149G=	NP_001138881.1:n.1282-149G=
NM_001145410.2:c.1015-149G=	NP_001138882.1:n.1015-149G=