Canonical Allele Identifier: CA2821730932
Gene: NONO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71299887_71299888insTCC , CM000685.2:g.71299887_71299888insTCC GRCh38
NC_000023.10:g.70519737_70519738insTCC , CM000685.1:g.70519737_70519738insTCC GRCh37
NC_000023.9:g.70436462_70436463insTCC NCBI36
NG_046742.1:g.21696_21697insTCC
NG_054891.1:g.3613_3614insTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000276079.13:c.1282-55_1282-54insTCC MANE Select ENSP00000276079.8:n.1282-55_1282-54insTCC
ENST00000373856.8:c.1380-55_1380-54insTCC ENSP00000362963.4:n.1380-55_1380-54insTCC
ENST00000420903.6:c.1282-55_1282-54insTCC ENSP00000410299.2:n.1282-55_1282-54insTCC
ENST00000450092.6:c.1282-55_1282-54insTCC ENSP00000415777.2:n.1282-55_1282-54insTCC
ENST00000454976.2:c.1282-55_1282-54insTCC ENSP00000406673.2:n.1282-55_1282-54insTCC
ENST00000473525.2:n.1990-55_1990-54insTCC
ENST00000676495.1:n.2693-55_2693-54insTCC
ENST00000676499.1:n.2238-55_2238-54insTCC
ENST00000676797.1:c.1015-55_1015-54insTCC ENSP00000503920.1:n.1015-55_1015-54insTCC
ENST00000677014.1:c.*1109-55_*1109-54insTCC ENSP00000503813.1:n.*1109-55_*1109-54insTCC
ENST00000677218.1:n.2453-55_2453-54insTCC
ENST00000677245.1:c.*1491-55_*1491-54insTCC ENSP00000503929.1:n.*1491-55_*1491-54insTCC
ENST00000677274.1:c.1282-55_1282-54insTCC ENSP00000504314.1:n.1282-55_1282-54insTCC
ENST00000677446.1:c.1282-55_1282-54insTCC ENSP00000503031.1:n.1282-55_1282-54insTCC
ENST00000677612.1:c.1282-55_1282-54insTCC ENSP00000504351.1:n.1282-55_1282-54insTCC
ENST00000677766.1:n.3632_3633insTCC
ENST00000677826.1:n.2024-55_2024-54insTCC
ENST00000677879.1:c.1102-55_1102-54insTCC ENSP00000504090.1:n.1102-55_1102-54insTCC
ENST00000677977.1:n.3114-55_3114-54insTCC
ENST00000678231.1:c.1282-55_1282-54insTCC ENSP00000503233.1:n.1282-55_1282-54insTCC
ENST00000678323.1:n.2380-55_2380-54insTCC
ENST00000678335.1:c.*195-55_*195-54insTCC ENSP00000503769.1:n.*195-55_*195-54insTCC
ENST00000678437.1:c.1273-55_1273-54insTCC ENSP00000504007.1:n.1273-55_1273-54insTCC
ENST00000678660.1:c.1297-55_1297-54insTCC ENSP00000504665.1:n.1297-55_1297-54insTCC
ENST00000678830.1:c.1372-55_1372-54insTCC ENSP00000504263.1:n.1372-55_1372-54insTCC
ENST00000679029.1:c.*96-55_*96-54insTCC ENSP00000504193.1:n.*96-55_*96-54insTCC
ENST00000679267.1:n.3434_3435insTCC
ENST00000276079.12:c.1282-55_1282-54insTCC ENSP00000276079.8:n.1282-55_1282-54insTCC
ENST00000373841.5:c.1282-55_1282-54insTCC ENSP00000362947.1:n.1282-55_1282-54insTCC
ENST00000373856.7:c.1282-55_1282-54insTCC ENSP00000362963.3:n.1282-55_1282-54insTCC
ENST00000472185.1:n.61-632_61-631insTCC
ENST00000473525.1:n.1056-55_1056-54insTCC
ENST00000474431.5:n.317-55_317-54insTCC
ENST00000490044.5:n.1989-55_1989-54insTCC
ENST00000535149.5:c.1015-55_1015-54insTCC ENSP00000441364.1:n.1015-55_1015-54insTCC
NM_001145408.1:c.1282-55_1282-54insTCC NP_001138880.1:n.1282-55_1282-54insTCC
NM_001145409.1:c.1282-55_1282-54insTCC NP_001138881.1:n.1282-55_1282-54insTCC
NM_001145410.1:c.1015-55_1015-54insTCC NP_001138882.1:n.1015-55_1015-54insTCC
NM_007363.4:c.1282-55_1282-54insTCC NP_031389.3:n.1282-55_1282-54insTCC
NM_007363.5:c.1282-55_1282-54insTCC MANE Select NP_031389.3:n.1282-55_1282-54insTCC
NM_001145408.2:c.1282-55_1282-54insTCC NP_001138880.1:n.1282-55_1282-54insTCC
NM_001145409.2:c.1282-55_1282-54insTCC NP_001138881.1:n.1282-55_1282-54insTCC
NM_001145410.2:c.1015-55_1015-54insTCC NP_001138882.1:n.1015-55_1015-54insTCC