Canonical Allele Identifier: CA2821730953

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300126dup , CM000685.2:g.71300126dup	GRCh38
NC_000023.10:g.70519976dup , CM000685.1:g.70519976dup	GRCh37
NC_000023.9:g.70436701dup	NCBI36
NG_046742.1:g.21935dup
NG_054891.1:g.3852dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*50dup MANE Select	ENSP00000276079.8:n.*50dup
ENST00000420903.6:c.*50dup	ENSP00000410299.2:n.*50dup
ENST00000473525.2:n.2174dup
ENST00000676495.1:n.2877dup
ENST00000676499.1:n.2422dup
ENST00000676797.1:c.*50dup	ENSP00000503920.1:n.*50dup
ENST00000677014.1:c.*1293dup	ENSP00000503813.1:n.*1293dup
ENST00000677218.1:n.2637dup
ENST00000677245.1:c.*1675dup	ENSP00000503929.1:n.*1675dup
ENST00000677274.1:c.*50dup	ENSP00000504314.1:n.*50dup
ENST00000677446.1:c.*50dup	ENSP00000503031.1:n.*50dup
ENST00000677612.1:c.*50dup	ENSP00000504351.1:n.*50dup
ENST00000677766.1:n.3871dup
ENST00000677826.1:n.2208dup
ENST00000677879.1:c.*50dup	ENSP00000504090.1:n.*50dup
ENST00000677977.1:n.3298dup
ENST00000678231.1:c.*50dup	ENSP00000503233.1:n.*50dup
ENST00000678323.1:n.2564dup
ENST00000678335.1:c.*379dup	ENSP00000503769.1:n.*379dup
ENST00000678437.1:c.*50dup	ENSP00000504007.1:n.*50dup
ENST00000678660.1:c.*50dup	ENSP00000504665.1:n.*50dup
ENST00000678830.1:c.*50dup	ENSP00000504263.1:n.*50dup
ENST00000679029.1:c.*280dup	ENSP00000504193.1:n.*280dup
ENST00000679267.1:n.3673dup
ENST00000276079.12:c.*50dup	ENSP00000276079.8:n.*50dup
ENST00000373841.5:c.*50dup	ENSP00000362947.1:n.*50dup
ENST00000373856.7:c.*50dup	ENSP00000362963.3:n.*50dup
ENST00000472185.1:n.61-393dup
ENST00000473525.1:n.1240dup
ENST00000474431.5:n.501dup
ENST00000490044.5:n.2173dup
ENST00000535149.5:c.*50dup	ENSP00000441364.1:n.*50dup
NM_001145408.1:c.*50dup	NP_001138880.1:n.*50dup
NM_001145409.1:c.*50dup	NP_001138881.1:n.*50dup
NM_001145410.1:c.*50dup	NP_001138882.1:n.*50dup
NM_007363.4:c.*50dup	NP_031389.3:n.*50dup
NM_007363.5:c.*50dup MANE Select	NP_031389.3:n.*50dup
NM_001145408.2:c.*50dup	NP_001138880.1:n.*50dup
NM_001145409.2:c.*50dup	NP_001138881.1:n.*50dup
NM_001145410.2:c.*50dup	NP_001138882.1:n.*50dup