Canonical Allele Identifier: CA2436414879
Gene: NONO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71300050G= , CM000685.2:g.71300050G= GRCh38
NC_000023.10:g.70519900G= , CM000685.1:g.70519900G= GRCh37
NC_000023.9:g.70436625G= NCBI36
NG_046742.1:g.21859G=
NG_054891.1:g.3776G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000276079.13:c.1390G= MANE Select ENSP00000276079.8:p.Ala464=
ENST00000373856.8:c.1488G= ENSP00000362963.4:p.Leu496=
ENST00000420903.6:c.1390G= ENSP00000410299.2:p.Ala464=
ENST00000450092.6:c.1390G= ENSP00000415777.2:p.Ala464=
ENST00000454976.2:c.1390G= ENSP00000406673.2:p.Ala464=
ENST00000473525.2:n.2098G=
ENST00000676495.1:n.2801G=
ENST00000676499.1:n.2346G=
ENST00000676797.1:c.1123G= ENSP00000503920.1:p.Ala375=
ENST00000677014.1:c.*1217G= ENSP00000503813.1:n.*1217G=
ENST00000677218.1:n.2561G=
ENST00000677245.1:c.*1599G= ENSP00000503929.1:n.*1599G=
ENST00000677274.1:c.1390G= ENSP00000504314.1:p.Ala464=
ENST00000677446.1:c.1390G= ENSP00000503031.1:p.Ala464=
ENST00000677612.1:c.1390G= ENSP00000504351.1:p.Ala464=
ENST00000677766.1:n.3795G=
ENST00000677826.1:n.2132G=
ENST00000677879.1:c.1210G= ENSP00000504090.1:p.Ala404=
ENST00000677977.1:n.3222G=
ENST00000678231.1:c.1390G= ENSP00000503233.1:p.Ala464=
ENST00000678323.1:n.2488G=
ENST00000678335.1:c.*303G= ENSP00000503769.1:n.*303G=
ENST00000678437.1:c.1381G= ENSP00000504007.1:p.Ala461=
ENST00000678660.1:c.1405G= ENSP00000504665.1:p.Ala469=
ENST00000678830.1:c.1480G= ENSP00000504263.1:p.Ala494=
ENST00000679029.1:c.*204G= ENSP00000504193.1:n.*204G=
ENST00000679267.1:n.3597G=
ENST00000276079.12:c.1390G= ENSP00000276079.8:p.Ala464=
ENST00000373841.5:c.1390G= ENSP00000362947.1:p.Ala464=
ENST00000373856.7:c.1390G= ENSP00000362963.3:p.Ala464=
ENST00000472185.1:n.61-469G=
ENST00000473525.1:n.1164G=
ENST00000474431.5:n.425G=
ENST00000490044.5:n.2097G=
ENST00000535149.5:c.1123G= ENSP00000441364.1:p.Ala375=
NM_001145408.1:c.1390G= NP_001138880.1:p.Ala464=
NM_001145409.1:c.1390G= NP_001138881.1:p.Ala464=
NM_001145410.1:c.1123G= NP_001138882.1:p.Ala375=
NM_007363.4:c.1390G= NP_031389.3:p.Ala464=
NM_007363.5:c.1390G= MANE Select NP_031389.3:p.Ala464=
NM_001145408.2:c.1390G= NP_001138880.1:p.Ala464=
NM_001145409.2:c.1390G= NP_001138881.1:p.Ala464=
NM_001145410.2:c.1123G= NP_001138882.1:p.Ala375=