Canonical Allele Identifier: CA2436411641
Gene: NONO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71290745G= , CM000685.2:g.71290745G= GRCh38
NC_000023.10:g.70510595G= , CM000685.1:g.70510595G= GRCh37
NC_000023.9:g.70427320G= NCBI36
NG_046742.1:g.12554G=

Transcript Alleles

HGVS Amino-acid change
ENST00000276079.13:c.108G= MANE Select ENSP00000276079.8:p.Pro36=
ENST00000373856.8:c.108G= ENSP00000362963.4:p.Pro36=
ENST00000420903.6:c.108G= ENSP00000410299.2:p.Pro36=
ENST00000450092.6:c.108G= ENSP00000415777.2:p.Pro36=
ENST00000454976.2:c.108G= ENSP00000406673.2:p.Pro36=
ENST00000471419.7:n.233G=
ENST00000473525.2:n.286G=
ENST00000676495.1:n.286G=
ENST00000676499.1:n.286G=
ENST00000676797.1:c.-160G= ENSP00000503920.1:n.-160G=
ENST00000677014.1:c.108G= ENSP00000503813.1:p.Pro36=
ENST00000677218.1:n.375G=
ENST00000677245.1:c.108G= ENSP00000503929.1:p.Pro36=
ENST00000677274.1:c.108G= ENSP00000504314.1:p.Pro36=
ENST00000677446.1:c.108G= ENSP00000503031.1:p.Pro36=
ENST00000677612.1:c.108G= ENSP00000504351.1:p.Pro36=
ENST00000677766.1:n.286G=
ENST00000677826.1:n.286G=
ENST00000677879.1:c.108G= ENSP00000504090.1:p.Pro36=
ENST00000677977.1:n.233G=
ENST00000678231.1:c.108G= ENSP00000503233.1:p.Pro36=
ENST00000678323.1:n.286G=
ENST00000678335.1:c.108G= ENSP00000503769.1:p.Pro36=
ENST00000678437.1:c.108G= ENSP00000504007.1:p.Pro36=
ENST00000678660.1:c.108G= ENSP00000504665.1:p.Pro36=
ENST00000678830.1:c.108G= ENSP00000504263.1:p.Pro36=
ENST00000679029.1:c.108G= ENSP00000504193.1:p.Pro36=
ENST00000679062.1:n.195G=
ENST00000679254.1:n.283G=
ENST00000679267.1:n.286G=
ENST00000276079.12:c.108G= ENSP00000276079.8:p.Pro36=
ENST00000373841.5:c.108G= ENSP00000362947.1:p.Pro36=
ENST00000373856.7:c.108G= ENSP00000362963.3:p.Pro36=
ENST00000413858.5:c.108G= ENSP00000413350.1:p.Pro36=
ENST00000420903.5:c.108G= ENSP00000410299.1:p.Pro36=
ENST00000450092.5:c.108G= ENSP00000415777.1:p.Pro36=
ENST00000454976.1:c.108G= ENSP00000406673.1:p.Pro36=
ENST00000472185.1:n.60+6339G=
ENST00000474431.5:n.70+7024G=
ENST00000486613.6:n.202G=
ENST00000535149.5:c.-113-1034G= ENSP00000441364.1:n.-113-1034G=
NM_001145408.1:c.108G= NP_001138880.1:p.Pro36=
NM_001145409.1:c.108G= NP_001138881.1:p.Pro36=
NM_001145410.1:c.-113-1034G= NP_001138882.1:n.-113-1034G=
NM_007363.4:c.108G= NP_031389.3:p.Pro36=
NM_007363.5:c.108G= MANE Select NP_031389.3:p.Pro36=
NM_001145408.2:c.108G= NP_001138880.1:p.Pro36=
NM_001145409.2:c.108G= NP_001138881.1:p.Pro36=
NM_001145410.2:c.-113-1034G= NP_001138882.1:n.-113-1034G=