Canonical Allele Identifier: CA2436411995
Gene: NONO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71291778G= , CM000685.2:g.71291778G= GRCh38
NC_000023.10:g.70511628G= , CM000685.1:g.70511628G= GRCh37
NC_000023.9:g.70428353G= NCBI36
NG_046742.1:g.13587G=

Transcript Alleles

HGVS Amino-acid change
ENST00000276079.13:c.155-1G= MANE Select ENSP00000276079.8:n.155-1G=
ENST00000373856.8:c.155-1G= ENSP00000362963.4:n.155-1G=
ENST00000420903.6:c.155-1G= ENSP00000410299.2:n.155-1G=
ENST00000450092.6:c.155-1G= ENSP00000415777.2:n.155-1G=
ENST00000454976.2:c.155-1G= ENSP00000406673.2:n.155-1G=
ENST00000471419.7:n.1266G=
ENST00000473525.2:n.333-1G=
ENST00000676495.1:n.333-1G=
ENST00000676499.1:n.333-1G=
ENST00000676797.1:c.-113-1G= ENSP00000503920.1:n.-113-1G=
ENST00000677014.1:c.159-7G= ENSP00000503813.1:n.159-7G=
ENST00000677218.1:n.422-1G=
ENST00000677245.1:c.155-1G= ENSP00000503929.1:n.155-1G=
ENST00000677274.1:c.155-1G= ENSP00000504314.1:n.155-1G=
ENST00000677446.1:c.155-1G= ENSP00000503031.1:n.155-1G=
ENST00000677612.1:c.155-1G= ENSP00000504351.1:n.155-1G=
ENST00000677766.1:n.333-1G=
ENST00000677826.1:n.333-1G=
ENST00000677879.1:c.155-1G= ENSP00000504090.1:n.155-1G=
ENST00000677977.1:n.1266G=
ENST00000678231.1:c.155-1G= ENSP00000503233.1:n.155-1G=
ENST00000678323.1:n.333-1G=
ENST00000678335.1:c.155-1G= ENSP00000503769.1:n.155-1G=
ENST00000678437.1:c.155-1G= ENSP00000504007.1:n.155-1G=
ENST00000678660.1:c.170-1G= ENSP00000504665.1:n.170-1G=
ENST00000678830.1:c.155-1G= ENSP00000504263.1:n.155-1G=
ENST00000679029.1:c.155-1G= ENSP00000504193.1:n.155-1G=
ENST00000679062.1:n.1228G=
ENST00000679254.1:n.1316G=
ENST00000679267.1:n.333-1G=
ENST00000276079.12:c.155-1G= ENSP00000276079.8:n.155-1G=
ENST00000373841.5:c.155-1G= ENSP00000362947.1:n.155-1G=
ENST00000373856.7:c.155-1G= ENSP00000362963.3:n.155-1G=
ENST00000413858.5:c.155-1G= ENSP00000413350.1:n.155-1G=
ENST00000420903.5:c.155-1G= ENSP00000410299.1:n.155-1G=
ENST00000450092.5:c.155-1G= ENSP00000415777.1:n.155-1G=
ENST00000454976.1:c.155-1G= ENSP00000406673.1:n.155-1G=
ENST00000472185.1:n.60+7372G=
ENST00000474431.5:n.71-6065G=
ENST00000486613.6:n.249-1G=
ENST00000535149.5:c.-113-1G= ENSP00000441364.1:n.-113-1G=
NM_001145408.1:c.155-1G= NP_001138880.1:n.155-1G=
NM_001145409.1:c.155-1G= NP_001138881.1:n.155-1G=
NM_001145410.1:c.-113-1G= NP_001138882.1:n.-113-1G=
NM_007363.4:c.155-1G= NP_031389.3:n.155-1G=
NM_007363.5:c.155-1G= MANE Select NP_031389.3:n.155-1G=
NM_001145408.2:c.155-1G= NP_001138880.1:n.155-1G=
NM_001145409.2:c.155-1G= NP_001138881.1:n.155-1G=
NM_001145410.2:c.-113-1G= NP_001138882.1:n.-113-1G=