Canonical Allele Identifier: CA2436414855

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299947_71299948delinsAC , CM000685.2:g.71299947_71299948delinsAC	GRCh38
NC_000023.10:g.70519797_70519798delinsAC , CM000685.1:g.70519797_70519798delinsAC	GRCh37
NC_000023.9:g.70436522_70436523delinsAC	NCBI36
NG_046742.1:g.21756_21757delinsAC
NG_054891.1:g.3673_3674delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1287_1288delinsAC MANE Select	ENSP00000276079.8:p.Pro429=
ENST00000373856.8:c.1385_1386delinsAC	ENSP00000362963.4:p.His462=
ENST00000420903.6:c.1287_1288delinsAC	ENSP00000410299.2:p.Pro429=
ENST00000450092.6:c.1287_1288delinsAC	ENSP00000415777.2:p.Pro429=
ENST00000454976.2:c.1287_1288delinsAC	ENSP00000406673.2:p.Pro429=
ENST00000473525.2:n.1995_1996delinsAC
ENST00000676495.1:n.2698_2699delinsAC
ENST00000676499.1:n.2243_2244delinsAC
ENST00000676797.1:c.1020_1021delinsAC	ENSP00000503920.1:p.Pro340=
ENST00000677014.1:c.*1114_*1115delinsAC	ENSP00000503813.1:n.*1114_*1115delinsAC
ENST00000677218.1:n.2458_2459delinsAC
ENST00000677245.1:c.*1496_*1497delinsAC	ENSP00000503929.1:n.*1496_*1497delinsAC
ENST00000677274.1:c.1287_1288delinsAC	ENSP00000504314.1:p.Pro429=
ENST00000677446.1:c.1287_1288delinsAC	ENSP00000503031.1:p.Pro429=
ENST00000677612.1:c.1287_1288delinsAC	ENSP00000504351.1:p.Pro429=
ENST00000677766.1:n.3692_3693delinsAC
ENST00000677826.1:n.2029_2030delinsAC
ENST00000677879.1:c.1107_1108delinsAC	ENSP00000504090.1:p.Pro369=
ENST00000677977.1:n.3119_3120delinsAC
ENST00000678231.1:c.1287_1288delinsAC	ENSP00000503233.1:p.Pro429=
ENST00000678323.1:n.2385_2386delinsAC
ENST00000678335.1:c.*200_*201delinsAC	ENSP00000503769.1:n.*200_*201delinsAC
ENST00000678437.1:c.1278_1279delinsAC	ENSP00000504007.1:p.Pro426=
ENST00000678660.1:c.1302_1303delinsAC	ENSP00000504665.1:p.Pro434=
ENST00000678830.1:c.1377_1378delinsAC	ENSP00000504263.1:p.Pro459=
ENST00000679029.1:c.*101_*102delinsAC	ENSP00000504193.1:n.*101_*102delinsAC
ENST00000679267.1:n.3494_3495delinsAC
ENST00000276079.12:c.1287_1288delinsAC	ENSP00000276079.8:p.Pro429=
ENST00000373841.5:c.1287_1288delinsAC	ENSP00000362947.1:p.Pro429=
ENST00000373856.7:c.1287_1288delinsAC	ENSP00000362963.3:p.Pro429=
ENST00000472185.1:n.61-572_61-571delinsAC
ENST00000473525.1:n.1061_1062delinsAC
ENST00000474431.5:n.322_323delinsAC
ENST00000490044.5:n.1994_1995delinsAC
ENST00000535149.5:c.1020_1021delinsAC	ENSP00000441364.1:p.Pro340=
NM_001145408.1:c.1287_1288delinsAC	NP_001138880.1:p.Pro429=
NM_001145409.1:c.1287_1288delinsAC	NP_001138881.1:p.Pro429=
NM_001145410.1:c.1020_1021delinsAC	NP_001138882.1:p.Pro340=
NM_007363.4:c.1287_1288delinsAC	NP_031389.3:p.Pro429=
NM_007363.5:c.1287_1288delinsAC MANE Select	NP_031389.3:p.Pro429=
NM_001145408.2:c.1287_1288delinsAC	NP_001138880.1:p.Pro429=
NM_001145409.2:c.1287_1288delinsAC	NP_001138881.1:p.Pro429=
NM_001145410.2:c.1020_1021delinsAC	NP_001138882.1:p.Pro340=