Canonical Allele Identifier: CA2436414928
Gene: NONO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71300187C= , CM000685.2:g.71300187C= GRCh38
NC_000023.10:g.70520037C= , CM000685.1:g.70520037C= GRCh37
NC_000023.9:g.70436762C= NCBI36
NG_046742.1:g.21996C=
NG_054891.1:g.3913C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000276079.13:c.*111C= MANE Select ENSP00000276079.8:n.*111C=
ENST00000420903.6:c.*111C= ENSP00000410299.2:n.*111C=
ENST00000473525.2:n.2235C=
ENST00000676495.1:n.2938C=
ENST00000676499.1:n.2483C=
ENST00000676797.1:c.*111C= ENSP00000503920.1:n.*111C=
ENST00000677014.1:c.*1354C= ENSP00000503813.1:n.*1354C=
ENST00000677218.1:n.2698C=
ENST00000677245.1:c.*1736C= ENSP00000503929.1:n.*1736C=
ENST00000677274.1:c.*111C= ENSP00000504314.1:n.*111C=
ENST00000677446.1:c.*111C= ENSP00000503031.1:n.*111C=
ENST00000677612.1:c.*111C= ENSP00000504351.1:n.*111C=
ENST00000677766.1:n.3932C=
ENST00000677826.1:n.2269C=
ENST00000677879.1:c.*111C= ENSP00000504090.1:n.*111C=
ENST00000677977.1:n.3359C=
ENST00000678231.1:c.*111C= ENSP00000503233.1:n.*111C=
ENST00000678323.1:n.2625C=
ENST00000678335.1:c.*440C= ENSP00000503769.1:n.*440C=
ENST00000678437.1:c.*111C= ENSP00000504007.1:n.*111C=
ENST00000678660.1:c.*111C= ENSP00000504665.1:n.*111C=
ENST00000678830.1:c.*111C= ENSP00000504263.1:n.*111C=
ENST00000679029.1:c.*341C= ENSP00000504193.1:n.*341C=
ENST00000679267.1:n.3734C=
ENST00000276079.12:c.*111C= ENSP00000276079.8:n.*111C=
ENST00000373841.5:c.*111C= ENSP00000362947.1:n.*111C=
ENST00000373856.7:c.*111C= ENSP00000362963.3:n.*111C=
ENST00000472185.1:n.61-332C=
ENST00000473525.1:n.1301C=
ENST00000474431.5:n.562C=
ENST00000490044.5:n.2234C=
ENST00000535149.5:c.*111C= ENSP00000441364.1:n.*111C=
NM_001145408.1:c.*111C= NP_001138880.1:n.*111C=
NM_001145409.1:c.*111C= NP_001138881.1:n.*111C=
NM_001145410.1:c.*111C= NP_001138882.1:n.*111C=
NM_007363.4:c.*111C= NP_031389.3:n.*111C=
NM_007363.5:c.*111C= MANE Select NP_031389.3:n.*111C=
NM_001145408.2:c.*111C= NP_001138880.1:n.*111C=
NM_001145409.2:c.*111C= NP_001138881.1:n.*111C=
NM_001145410.2:c.*111C= NP_001138882.1:n.*111C=