Canonical Allele Identifier: CA413550150

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519826C>A (hg19) ; chrX:g.71299976C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299976C>A , CM000685.2:g.71299976C>A	GRCh38
NC_000023.10:g.70519826C>A , CM000685.1:g.70519826C>A	GRCh37
NC_000023.9:g.70436551C>A	NCBI36
NG_046742.1:g.21785C>A
NG_054891.1:g.3702C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1316C>A MANE Select	ENSP00000276079.8:p.Ala439Asp
ENST00000373856.8:c.1414C>A	ENSP00000362963.4:p.Leu472Ile
ENST00000420903.6:c.1316C>A	ENSP00000410299.2:p.Ala439Asp
ENST00000450092.6:c.1316C>A	ENSP00000415777.2:p.Ala439Asp
ENST00000454976.2:c.1316C>A	ENSP00000406673.2:p.Ala439Asp
ENST00000473525.2:n.2024C>A
ENST00000676495.1:n.2727C>A
ENST00000676499.1:n.2272C>A
ENST00000676797.1:c.1049C>A	ENSP00000503920.1:p.Ala350Asp
ENST00000677014.1:c.*1143C>A	ENSP00000503813.1:n.*1143C>A
ENST00000677218.1:n.2487C>A
ENST00000677245.1:c.*1525C>A	ENSP00000503929.1:n.*1525C>A
ENST00000677274.1:c.1316C>A	ENSP00000504314.1:p.Ala439Asp
ENST00000677446.1:c.1316C>A	ENSP00000503031.1:p.Ala439Asp
ENST00000677612.1:c.1316C>A	ENSP00000504351.1:p.Ala439Asp
ENST00000677766.1:n.3721C>A
ENST00000677826.1:n.2058C>A
ENST00000677879.1:c.1136C>A	ENSP00000504090.1:p.Ala379Asp
ENST00000677977.1:n.3148C>A
ENST00000678231.1:c.1316C>A	ENSP00000503233.1:p.Ala439Asp
ENST00000678323.1:n.2414C>A
ENST00000678335.1:c.*229C>A	ENSP00000503769.1:n.*229C>A
ENST00000678437.1:c.1307C>A	ENSP00000504007.1:p.Ala436Asp
ENST00000678660.1:c.1331C>A	ENSP00000504665.1:p.Ala444Asp
ENST00000678830.1:c.1406C>A	ENSP00000504263.1:p.Ala469Asp
ENST00000679029.1:c.*130C>A	ENSP00000504193.1:n.*130C>A
ENST00000679267.1:n.3523C>A
ENST00000276079.12:c.1316C>A	ENSP00000276079.8:p.Ala439Asp
ENST00000373841.5:c.1316C>A	ENSP00000362947.1:p.Ala439Asp
ENST00000373856.7:c.1316C>A	ENSP00000362963.3:p.Ala439Asp
ENST00000472185.1:n.61-543C>A
ENST00000473525.1:n.1090C>A
ENST00000474431.5:n.351C>A
ENST00000490044.5:n.2023C>A
ENST00000535149.5:c.1049C>A	ENSP00000441364.1:p.Ala350Asp
NM_001145408.1:c.1316C>A	NP_001138880.1:p.Ala439Asp
NM_001145409.1:c.1316C>A	NP_001138881.1:p.Ala439Asp
NM_001145410.1:c.1049C>A	NP_001138882.1:p.Ala350Asp
NM_007363.4:c.1316C>A	NP_031389.3:p.Ala439Asp
NM_007363.5:c.1316C>A MANE Select	NP_031389.3:p.Ala439Asp
NM_001145408.2:c.1316C>A	NP_001138880.1:p.Ala439Asp
NM_001145409.2:c.1316C>A	NP_001138881.1:p.Ala439Asp
NM_001145410.2:c.1049C>A	NP_001138882.1:p.Ala350Asp