Canonical Allele Identifier: CA2436414965
Gene: NONO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71300312A= , CM000685.2:g.71300312A= GRCh38
NC_000023.10:g.70520162A= , CM000685.1:g.70520162A= GRCh37
NC_000023.9:g.70436887A= NCBI36
NG_046742.1:g.22121A=
NG_054891.1:g.4038A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000276079.13:c.*236A= MANE Select ENSP00000276079.8:n.*236A=
ENST00000420903.6:c.*236A= ENSP00000410299.2:n.*236A=
ENST00000473525.2:n.2360A=
ENST00000676495.1:n.3063A=
ENST00000676499.1:n.2608A=
ENST00000676797.1:c.*236A= ENSP00000503920.1:n.*236A=
ENST00000677014.1:c.*1479A= ENSP00000503813.1:n.*1479A=
ENST00000677218.1:n.2823A=
ENST00000677245.1:c.*1861A= ENSP00000503929.1:n.*1861A=
ENST00000677274.1:c.*236A= ENSP00000504314.1:n.*236A=
ENST00000677446.1:c.*236A= ENSP00000503031.1:n.*236A=
ENST00000677612.1:c.*236A= ENSP00000504351.1:n.*236A=
ENST00000677766.1:n.4057A=
ENST00000677826.1:n.2394A=
ENST00000677879.1:c.*236A= ENSP00000504090.1:n.*236A=
ENST00000677977.1:n.3484A=
ENST00000678231.1:c.*236A= ENSP00000503233.1:n.*236A=
ENST00000678323.1:n.2750A=
ENST00000678335.1:c.*565A= ENSP00000503769.1:n.*565A=
ENST00000678437.1:c.*236A= ENSP00000504007.1:n.*236A=
ENST00000678660.1:c.*236A= ENSP00000504665.1:n.*236A=
ENST00000678830.1:c.*236A= ENSP00000504263.1:n.*236A=
ENST00000679029.1:c.*466A= ENSP00000504193.1:n.*466A=
ENST00000679267.1:n.3859A=
ENST00000276079.12:c.*236A= ENSP00000276079.8:n.*236A=
ENST00000373841.5:c.*236A= ENSP00000362947.1:n.*236A=
ENST00000472185.1:n.61-207A=
ENST00000473525.1:n.1426A=
ENST00000490044.5:n.2359A=
ENST00000535149.5:c.*236A= ENSP00000441364.1:n.*236A=
NM_001145408.1:c.*236A= NP_001138880.1:n.*236A=
NM_001145409.1:c.*236A= NP_001138881.1:n.*236A=
NM_001145410.1:c.*236A= NP_001138882.1:n.*236A=
NM_007363.4:c.*236A= NP_031389.3:n.*236A=
NM_007363.5:c.*236A= MANE Select NP_031389.3:n.*236A=
NM_001145408.2:c.*236A= NP_001138880.1:n.*236A=
NM_001145409.2:c.*236A= NP_001138881.1:n.*236A=
NM_001145410.2:c.*236A= NP_001138882.1:n.*236A=