Canonical Allele Identifier: CA2821730966

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300325_71300327del , CM000685.2:g.71300325_71300327del	GRCh38
NC_000023.10:g.70520175_70520177del , CM000685.1:g.70520175_70520177del	GRCh37
NC_000023.9:g.70436900_70436902del	NCBI36
NG_046742.1:g.22134_22136del
NG_054891.1:g.4051_4053del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*249_*251del MANE Select	ENSP00000276079.8:n.*249_*251del
ENST00000420903.6:c.*249_*251del	ENSP00000410299.2:n.*249_*251del
ENST00000473525.2:n.2373_2375del
ENST00000676495.1:n.3076_3078del
ENST00000676499.1:n.2621_2623del
ENST00000676797.1:c.*249_*251del	ENSP00000503920.1:n.*249_*251del
ENST00000677014.1:c.*1492_*1494del	ENSP00000503813.1:n.*1492_*1494del
ENST00000677218.1:n.2836_2838del
ENST00000677245.1:c.*1874_*1876del	ENSP00000503929.1:n.*1874_*1876del
ENST00000677274.1:c.*249_*251del	ENSP00000504314.1:n.*249_*251del
ENST00000677446.1:c.*249_*251del	ENSP00000503031.1:n.*249_*251del
ENST00000677612.1:c.*249_*251del	ENSP00000504351.1:n.*249_*251del
ENST00000677766.1:n.4070_4072del
ENST00000677826.1:n.2407_2409del
ENST00000677879.1:c.*249_*251del	ENSP00000504090.1:n.*249_*251del
ENST00000677977.1:n.3497_3499del
ENST00000678231.1:c.*249_*251del	ENSP00000503233.1:n.*249_*251del
ENST00000678323.1:n.2763_2765del
ENST00000678335.1:c.*578_*580del	ENSP00000503769.1:n.*578_*580del
ENST00000678437.1:c.*249_*251del	ENSP00000504007.1:n.*249_*251del
ENST00000678660.1:c.*249_*251del	ENSP00000504665.1:n.*249_*251del
ENST00000678830.1:c.*249_*251del	ENSP00000504263.1:n.*249_*251del
ENST00000679029.1:c.*479_*481del	ENSP00000504193.1:n.*479_*481del
ENST00000679267.1:n.3872_3874del
ENST00000276079.12:c.*249_*251del	ENSP00000276079.8:n.*249_*251del
ENST00000373841.5:c.*249_*251del	ENSP00000362947.1:n.*249_*251del
ENST00000472185.1:n.61-194_61-192del
ENST00000490044.5:n.2372_2374del
ENST00000535149.5:c.*249_*251del	ENSP00000441364.1:n.*249_*251del
NM_001145408.1:c.*249_*251del	NP_001138880.1:n.*249_*251del
NM_001145409.1:c.*249_*251del	NP_001138881.1:n.*249_*251del
NM_001145410.1:c.*249_*251del	NP_001138882.1:n.*249_*251del
NM_007363.4:c.*249_*251del	NP_031389.3:n.*249_*251del
NM_007363.5:c.*249_*251del MANE Select	NP_031389.3:n.*249_*251del
NM_001145408.2:c.*249_*251del	NP_001138880.1:n.*249_*251del
NM_001145409.2:c.*249_*251del	NP_001138881.1:n.*249_*251del
NM_001145410.2:c.*249_*251del	NP_001138882.1:n.*249_*251del