Canonical Allele Identifier: CA413550547

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519892C>A (hg19) ; chrX:g.71300042C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300042C>A , CM000685.2:g.71300042C>A	GRCh38
NC_000023.10:g.70519892C>A , CM000685.1:g.70519892C>A	GRCh37
NC_000023.9:g.70436617C>A	NCBI36
NG_046742.1:g.21851C>A
NG_054891.1:g.3768C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1382C>A MANE Select	ENSP00000276079.8:p.Ala461Asp
ENST00000373856.8:c.1480C>A	ENSP00000362963.4:p.Leu494Met
ENST00000420903.6:c.1382C>A	ENSP00000410299.2:p.Ala461Asp
ENST00000450092.6:c.1382C>A	ENSP00000415777.2:p.Ala461Asp
ENST00000454976.2:c.1382C>A	ENSP00000406673.2:p.Ala461Asp
ENST00000473525.2:n.2090C>A
ENST00000676495.1:n.2793C>A
ENST00000676499.1:n.2338C>A
ENST00000676797.1:c.1115C>A	ENSP00000503920.1:p.Ala372Asp
ENST00000677014.1:c.*1209C>A	ENSP00000503813.1:n.*1209C>A
ENST00000677218.1:n.2553C>A
ENST00000677245.1:c.*1591C>A	ENSP00000503929.1:n.*1591C>A
ENST00000677274.1:c.1382C>A	ENSP00000504314.1:p.Ala461Asp
ENST00000677446.1:c.1382C>A	ENSP00000503031.1:p.Ala461Asp
ENST00000677612.1:c.1382C>A	ENSP00000504351.1:p.Ala461Asp
ENST00000677766.1:n.3787C>A
ENST00000677826.1:n.2124C>A
ENST00000677879.1:c.1202C>A	ENSP00000504090.1:p.Ala401Asp
ENST00000677977.1:n.3214C>A
ENST00000678231.1:c.1382C>A	ENSP00000503233.1:p.Ala461Asp
ENST00000678323.1:n.2480C>A
ENST00000678335.1:c.*295C>A	ENSP00000503769.1:n.*295C>A
ENST00000678437.1:c.1373C>A	ENSP00000504007.1:p.Ala458Asp
ENST00000678660.1:c.1397C>A	ENSP00000504665.1:p.Ala466Asp
ENST00000678830.1:c.1472C>A	ENSP00000504263.1:p.Ala491Asp
ENST00000679029.1:c.*196C>A	ENSP00000504193.1:n.*196C>A
ENST00000679267.1:n.3589C>A
ENST00000276079.12:c.1382C>A	ENSP00000276079.8:p.Ala461Asp
ENST00000373841.5:c.1382C>A	ENSP00000362947.1:p.Ala461Asp
ENST00000373856.7:c.1382C>A	ENSP00000362963.3:p.Ala461Asp
ENST00000472185.1:n.61-477C>A
ENST00000473525.1:n.1156C>A
ENST00000474431.5:n.417C>A
ENST00000490044.5:n.2089C>A
ENST00000535149.5:c.1115C>A	ENSP00000441364.1:p.Ala372Asp
NM_001145408.1:c.1382C>A	NP_001138880.1:p.Ala461Asp
NM_001145409.1:c.1382C>A	NP_001138881.1:p.Ala461Asp
NM_001145410.1:c.1115C>A	NP_001138882.1:p.Ala372Asp
NM_007363.4:c.1382C>A	NP_031389.3:p.Ala461Asp
NM_007363.5:c.1382C>A MANE Select	NP_031389.3:p.Ala461Asp
NM_001145408.2:c.1382C>A	NP_001138880.1:p.Ala461Asp
NM_001145409.2:c.1382C>A	NP_001138881.1:p.Ala461Asp
NM_001145410.2:c.1115C>A	NP_001138882.1:p.Ala372Asp