Canonical Allele Identifier: CA2436414861

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299978A= , CM000685.2:g.71299978A=	GRCh38
NC_000023.10:g.70519828A= , CM000685.1:g.70519828A=	GRCh37
NC_000023.9:g.70436553A=	NCBI36
NG_046742.1:g.21787A=
NG_054891.1:g.3704A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1318A= MANE Select	ENSP00000276079.8:p.Thr440=
ENST00000373856.8:c.1416A=	ENSP00000362963.4:p.Leu472=
ENST00000420903.6:c.1318A=	ENSP00000410299.2:p.Thr440=
ENST00000450092.6:c.1318A=	ENSP00000415777.2:p.Thr440=
ENST00000454976.2:c.1318A=	ENSP00000406673.2:p.Thr440=
ENST00000473525.2:n.2026A=
ENST00000676495.1:n.2729A=
ENST00000676499.1:n.2274A=
ENST00000676797.1:c.1051A=	ENSP00000503920.1:p.Thr351=
ENST00000677014.1:c.*1145A=	ENSP00000503813.1:n.*1145A=
ENST00000677218.1:n.2489A=
ENST00000677245.1:c.*1527A=	ENSP00000503929.1:n.*1527A=
ENST00000677274.1:c.1318A=	ENSP00000504314.1:p.Thr440=
ENST00000677446.1:c.1318A=	ENSP00000503031.1:p.Thr440=
ENST00000677612.1:c.1318A=	ENSP00000504351.1:p.Thr440=
ENST00000677766.1:n.3723A=
ENST00000677826.1:n.2060A=
ENST00000677879.1:c.1138A=	ENSP00000504090.1:p.Thr380=
ENST00000677977.1:n.3150A=
ENST00000678231.1:c.1318A=	ENSP00000503233.1:p.Thr440=
ENST00000678323.1:n.2416A=
ENST00000678335.1:c.*231A=	ENSP00000503769.1:n.*231A=
ENST00000678437.1:c.1309A=	ENSP00000504007.1:p.Thr437=
ENST00000678660.1:c.1333A=	ENSP00000504665.1:p.Thr445=
ENST00000678830.1:c.1408A=	ENSP00000504263.1:p.Thr470=
ENST00000679029.1:c.*132A=	ENSP00000504193.1:n.*132A=
ENST00000679267.1:n.3525A=
ENST00000276079.12:c.1318A=	ENSP00000276079.8:p.Thr440=
ENST00000373841.5:c.1318A=	ENSP00000362947.1:p.Thr440=
ENST00000373856.7:c.1318A=	ENSP00000362963.3:p.Thr440=
ENST00000472185.1:n.61-541A=
ENST00000473525.1:n.1092A=
ENST00000474431.5:n.353A=
ENST00000490044.5:n.2025A=
ENST00000535149.5:c.1051A=	ENSP00000441364.1:p.Thr351=
NM_001145408.1:c.1318A=	NP_001138880.1:p.Thr440=
NM_001145409.1:c.1318A=	NP_001138881.1:p.Thr440=
NM_001145410.1:c.1051A=	NP_001138882.1:p.Thr351=
NM_007363.4:c.1318A=	NP_031389.3:p.Thr440=
NM_007363.5:c.1318A= MANE Select	NP_031389.3:p.Thr440=
NM_001145408.2:c.1318A=	NP_001138880.1:p.Thr440=
NM_001145409.2:c.1318A=	NP_001138881.1:p.Thr440=
NM_001145410.2:c.1051A=	NP_001138882.1:p.Thr351=