Canonical Allele Identifier: CA516732303

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519836A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299986A>G , CM000685.2:g.71299986A>G	GRCh38
NC_000023.10:g.70519836A>G , CM000685.1:g.70519836A>G	GRCh37
NC_000023.9:g.70436561A>G	NCBI36
NG_046742.1:g.21795A>G
NG_054891.1:g.3712A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1326A>G MANE Select	ENSP00000276079.8:p.Glu442=
ENST00000373856.8:c.1424A>G	ENSP00000362963.4:p.Lys475Arg
ENST00000420903.6:c.1326A>G	ENSP00000410299.2:p.Glu442=
ENST00000450092.6:c.1326A>G	ENSP00000415777.2:p.Glu442=
ENST00000454976.2:c.1326A>G	ENSP00000406673.2:p.Glu442=
ENST00000473525.2:n.2034A>G
ENST00000676495.1:n.2737A>G
ENST00000676499.1:n.2282A>G
ENST00000676797.1:c.1059A>G	ENSP00000503920.1:p.Glu353=
ENST00000677014.1:c.*1153A>G	ENSP00000503813.1:n.*1153A>G
ENST00000677218.1:n.2497A>G
ENST00000677245.1:c.*1535A>G	ENSP00000503929.1:n.*1535A>G
ENST00000677274.1:c.1326A>G	ENSP00000504314.1:p.Glu442=
ENST00000677446.1:c.1326A>G	ENSP00000503031.1:p.Glu442=
ENST00000677612.1:c.1326A>G	ENSP00000504351.1:p.Glu442=
ENST00000677766.1:n.3731A>G
ENST00000677826.1:n.2068A>G
ENST00000677879.1:c.1146A>G	ENSP00000504090.1:p.Glu382=
ENST00000677977.1:n.3158A>G
ENST00000678231.1:c.1326A>G	ENSP00000503233.1:p.Glu442=
ENST00000678323.1:n.2424A>G
ENST00000678335.1:c.*239A>G	ENSP00000503769.1:n.*239A>G
ENST00000678437.1:c.1317A>G	ENSP00000504007.1:p.Glu439=
ENST00000678660.1:c.1341A>G	ENSP00000504665.1:p.Glu447=
ENST00000678830.1:c.1416A>G	ENSP00000504263.1:p.Glu472=
ENST00000679029.1:c.*140A>G	ENSP00000504193.1:n.*140A>G
ENST00000679267.1:n.3533A>G
ENST00000276079.12:c.1326A>G	ENSP00000276079.8:p.Glu442=
ENST00000373841.5:c.1326A>G	ENSP00000362947.1:p.Glu442=
ENST00000373856.7:c.1326A>G	ENSP00000362963.3:p.Glu442=
ENST00000472185.1:n.61-533A>G
ENST00000473525.1:n.1100A>G
ENST00000474431.5:n.361A>G
ENST00000490044.5:n.2033A>G
ENST00000535149.5:c.1059A>G	ENSP00000441364.1:p.Glu353=
NM_001145408.1:c.1326A>G	NP_001138880.1:p.Glu442=
NM_001145409.1:c.1326A>G	NP_001138881.1:p.Glu442=
NM_001145410.1:c.1059A>G	NP_001138882.1:p.Glu353=
NM_007363.4:c.1326A>G	NP_031389.3:p.Glu442=
NM_007363.5:c.1326A>G MANE Select	NP_031389.3:p.Glu442=
NM_001145408.2:c.1326A>G	NP_001138880.1:p.Glu442=
NM_001145409.2:c.1326A>G	NP_001138881.1:p.Glu442=
NM_001145410.2:c.1059A>G	NP_001138882.1:p.Glu353=