Canonical Allele Identifier: CA2436414886
Gene: NONO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71300070A= , CM000685.2:g.71300070A= GRCh38
NC_000023.10:g.70519920A= , CM000685.1:g.70519920A= GRCh37
NC_000023.9:g.70436645A= NCBI36
NG_046742.1:g.21879A=
NG_054891.1:g.3796A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000276079.13:c.1410A= MANE Select ENSP00000276079.8:p.Arg470=
ENST00000373856.8:c.1508A= ENSP00000362963.4:p.Asp503=
ENST00000420903.6:c.1410A= ENSP00000410299.2:p.Arg470=
ENST00000450092.6:c.1410A= ENSP00000415777.2:p.Arg470=
ENST00000454976.2:c.1410A= ENSP00000406673.2:p.Arg470=
ENST00000473525.2:n.2118A=
ENST00000676495.1:n.2821A=
ENST00000676499.1:n.2366A=
ENST00000676797.1:c.1143A= ENSP00000503920.1:p.Arg381=
ENST00000677014.1:c.*1237A= ENSP00000503813.1:n.*1237A=
ENST00000677218.1:n.2581A=
ENST00000677245.1:c.*1619A= ENSP00000503929.1:n.*1619A=
ENST00000677274.1:c.1410A= ENSP00000504314.1:p.Arg470=
ENST00000677446.1:c.1410A= ENSP00000503031.1:p.Arg470=
ENST00000677612.1:c.1410A= ENSP00000504351.1:p.Arg470=
ENST00000677766.1:n.3815A=
ENST00000677826.1:n.2152A=
ENST00000677879.1:c.1230A= ENSP00000504090.1:p.Arg410=
ENST00000677977.1:n.3242A=
ENST00000678231.1:c.1410A= ENSP00000503233.1:p.Arg470=
ENST00000678323.1:n.2508A=
ENST00000678335.1:c.*323A= ENSP00000503769.1:n.*323A=
ENST00000678437.1:c.1401A= ENSP00000504007.1:p.Arg467=
ENST00000678660.1:c.1425A= ENSP00000504665.1:p.Arg475=
ENST00000678830.1:c.1500A= ENSP00000504263.1:p.Arg500=
ENST00000679029.1:c.*224A= ENSP00000504193.1:n.*224A=
ENST00000679267.1:n.3617A=
ENST00000276079.12:c.1410A= ENSP00000276079.8:p.Arg470=
ENST00000373841.5:c.1410A= ENSP00000362947.1:p.Arg470=
ENST00000373856.7:c.1410A= ENSP00000362963.3:p.Arg470=
ENST00000472185.1:n.61-449A=
ENST00000473525.1:n.1184A=
ENST00000474431.5:n.445A=
ENST00000490044.5:n.2117A=
ENST00000535149.5:c.1143A= ENSP00000441364.1:p.Arg381=
NM_001145408.1:c.1410A= NP_001138880.1:p.Arg470=
NM_001145409.1:c.1410A= NP_001138881.1:p.Arg470=
NM_001145410.1:c.1143A= NP_001138882.1:p.Arg381=
NM_007363.4:c.1410A= NP_031389.3:p.Arg470=
NM_007363.5:c.1410A= MANE Select NP_031389.3:p.Arg470=
NM_001145408.2:c.1410A= NP_001138880.1:p.Arg470=
NM_001145409.2:c.1410A= NP_001138881.1:p.Arg470=
NM_001145410.2:c.1143A= NP_001138882.1:p.Arg381=