Canonical Allele Identifier: CA2436414872
Gene: NONO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71300020T= , CM000685.2:g.71300020T= GRCh38
NC_000023.10:g.70519870T= , CM000685.1:g.70519870T= GRCh37
NC_000023.9:g.70436595T= NCBI36
NG_046742.1:g.21829T=
NG_054891.1:g.3746T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000276079.13:c.1360T= MANE Select ENSP00000276079.8:p.Phe454=
ENST00000373856.8:c.1458T= ENSP00000362963.4:p.His486=
ENST00000420903.6:c.1360T= ENSP00000410299.2:p.Phe454=
ENST00000450092.6:c.1360T= ENSP00000415777.2:p.Phe454=
ENST00000454976.2:c.1360T= ENSP00000406673.2:p.Phe454=
ENST00000473525.2:n.2068T=
ENST00000676495.1:n.2771T=
ENST00000676499.1:n.2316T=
ENST00000676797.1:c.1093T= ENSP00000503920.1:p.Phe365=
ENST00000677014.1:c.*1187T= ENSP00000503813.1:n.*1187T=
ENST00000677218.1:n.2531T=
ENST00000677245.1:c.*1569T= ENSP00000503929.1:n.*1569T=
ENST00000677274.1:c.1360T= ENSP00000504314.1:p.Phe454=
ENST00000677446.1:c.1360T= ENSP00000503031.1:p.Phe454=
ENST00000677612.1:c.1360T= ENSP00000504351.1:p.Phe454=
ENST00000677766.1:n.3765T=
ENST00000677826.1:n.2102T=
ENST00000677879.1:c.1180T= ENSP00000504090.1:p.Phe394=
ENST00000677977.1:n.3192T=
ENST00000678231.1:c.1360T= ENSP00000503233.1:p.Phe454=
ENST00000678323.1:n.2458T=
ENST00000678335.1:c.*273T= ENSP00000503769.1:n.*273T=
ENST00000678437.1:c.1351T= ENSP00000504007.1:p.Phe451=
ENST00000678660.1:c.1375T= ENSP00000504665.1:p.Phe459=
ENST00000678830.1:c.1450T= ENSP00000504263.1:p.Phe484=
ENST00000679029.1:c.*174T= ENSP00000504193.1:n.*174T=
ENST00000679267.1:n.3567T=
ENST00000276079.12:c.1360T= ENSP00000276079.8:p.Phe454=
ENST00000373841.5:c.1360T= ENSP00000362947.1:p.Phe454=
ENST00000373856.7:c.1360T= ENSP00000362963.3:p.Phe454=
ENST00000472185.1:n.61-499T=
ENST00000473525.1:n.1134T=
ENST00000474431.5:n.395T=
ENST00000490044.5:n.2067T=
ENST00000535149.5:c.1093T= ENSP00000441364.1:p.Phe365=
NM_001145408.1:c.1360T= NP_001138880.1:p.Phe454=
NM_001145409.1:c.1360T= NP_001138881.1:p.Phe454=
NM_001145410.1:c.1093T= NP_001138882.1:p.Phe365=
NM_007363.4:c.1360T= NP_031389.3:p.Phe454=
NM_007363.5:c.1360T= MANE Select NP_031389.3:p.Phe454=
NM_001145408.2:c.1360T= NP_001138880.1:p.Phe454=
NM_001145409.2:c.1360T= NP_001138881.1:p.Phe454=
NM_001145410.2:c.1093T= NP_001138882.1:p.Phe365=