Canonical Allele Identifier: CA2436414862

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299981A= , CM000685.2:g.71299981A=	GRCh38
NC_000023.10:g.70519831A= , CM000685.1:g.70519831A=	GRCh37
NC_000023.9:g.70436556A=	NCBI36
NG_046742.1:g.21790A=
NG_054891.1:g.3707A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1321A= MANE Select	ENSP00000276079.8:p.Met441=
ENST00000373856.8:c.1419A=	ENSP00000362963.4:p.Gln473=
ENST00000420903.6:c.1321A=	ENSP00000410299.2:p.Met441=
ENST00000450092.6:c.1321A=	ENSP00000415777.2:p.Met441=
ENST00000454976.2:c.1321A=	ENSP00000406673.2:p.Met441=
ENST00000473525.2:n.2029A=
ENST00000676495.1:n.2732A=
ENST00000676499.1:n.2277A=
ENST00000676797.1:c.1054A=	ENSP00000503920.1:p.Met352=
ENST00000677014.1:c.*1148A=	ENSP00000503813.1:n.*1148A=
ENST00000677218.1:n.2492A=
ENST00000677245.1:c.*1530A=	ENSP00000503929.1:n.*1530A=
ENST00000677274.1:c.1321A=	ENSP00000504314.1:p.Met441=
ENST00000677446.1:c.1321A=	ENSP00000503031.1:p.Met441=
ENST00000677612.1:c.1321A=	ENSP00000504351.1:p.Met441=
ENST00000677766.1:n.3726A=
ENST00000677826.1:n.2063A=
ENST00000677879.1:c.1141A=	ENSP00000504090.1:p.Met381=
ENST00000677977.1:n.3153A=
ENST00000678231.1:c.1321A=	ENSP00000503233.1:p.Met441=
ENST00000678323.1:n.2419A=
ENST00000678335.1:c.*234A=	ENSP00000503769.1:n.*234A=
ENST00000678437.1:c.1312A=	ENSP00000504007.1:p.Met438=
ENST00000678660.1:c.1336A=	ENSP00000504665.1:p.Met446=
ENST00000678830.1:c.1411A=	ENSP00000504263.1:p.Met471=
ENST00000679029.1:c.*135A=	ENSP00000504193.1:n.*135A=
ENST00000679267.1:n.3528A=
ENST00000276079.12:c.1321A=	ENSP00000276079.8:p.Met441=
ENST00000373841.5:c.1321A=	ENSP00000362947.1:p.Met441=
ENST00000373856.7:c.1321A=	ENSP00000362963.3:p.Met441=
ENST00000472185.1:n.61-538A=
ENST00000473525.1:n.1095A=
ENST00000474431.5:n.356A=
ENST00000490044.5:n.2028A=
ENST00000535149.5:c.1054A=	ENSP00000441364.1:p.Met352=
NM_001145408.1:c.1321A=	NP_001138880.1:p.Met441=
NM_001145409.1:c.1321A=	NP_001138881.1:p.Met441=
NM_001145410.1:c.1054A=	NP_001138882.1:p.Met352=
NM_007363.4:c.1321A=	NP_031389.3:p.Met441=
NM_007363.5:c.1321A= MANE Select	NP_031389.3:p.Met441=
NM_001145408.2:c.1321A=	NP_001138880.1:p.Met441=
NM_001145409.2:c.1321A=	NP_001138881.1:p.Met441=
NM_001145410.2:c.1054A=	NP_001138882.1:p.Met352=