Canonical Allele Identifier: CA2436414896

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300104_71300127delinsCCCTTAAAAGAAGGACCCTTTTTG , CM000685.2:g.71300104_71300127delinsCCCTTAAAAGAAGGACCCTTTTTG	GRCh38
NC_000023.10:g.70519954_70519977delinsCCCTTAAAAGAAGGACCCTTTTTG , CM000685.1:g.70519954_70519977delinsCCCTTAAAAGAAGGACCCTTTTTG	GRCh37
NC_000023.9:g.70436679_70436702delinsCCCTTAAAAGAAGGACCCTTTTTG	NCBI36
NG_046742.1:g.21913_21936delinsCCCTTAAAAGAAGGACCCTTTTTG
NG_054891.1:g.3830_3853delinsCCCTTAAAAGAAGGACCCTTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG MANE Select	ENSP00000276079.8:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000420903.6:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000410299.2:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000473525.2:n.2152_2175delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000676495.1:n.2855_2878delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000676499.1:n.2400_2423delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000676797.1:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000503920.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000677014.1:c.*1271_*1294delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000503813.1:n.*1271_*1294delinsCCCTTAAAAGAAGGACCCTTTTTG...
ENST00000677218.1:n.2615_2638delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000677245.1:c.*1653_*1676delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000503929.1:n.*1653_*1676delinsCCCTTAAAAGAAGGACCCTTTTTG...
ENST00000677274.1:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000504314.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000677446.1:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000503031.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000677612.1:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000504351.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000677766.1:n.3849_3872delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000677826.1:n.2186_2209delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000677879.1:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000504090.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000677977.1:n.3276_3299delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000678231.1:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000503233.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000678323.1:n.2542_2565delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000678335.1:c.*357_*380delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000503769.1:n.*357_*380delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000678437.1:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000504007.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000678660.1:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000504665.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000678830.1:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000504263.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000679029.1:c.*258_*281delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000504193.1:n.*258_*281delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000679267.1:n.3651_3674delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000276079.12:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000276079.8:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000373841.5:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000362947.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000373856.7:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000362963.3:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000472185.1:n.61-415_61-392delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000473525.1:n.1218_1241delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000474431.5:n.479_502delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000490044.5:n.2151_2174delinsCCCTTAAAAGAAGGACCCTTTTTG
ENST00000535149.5:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	ENSP00000441364.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
NM_001145408.1:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	NP_001138880.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
NM_001145409.1:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	NP_001138881.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
NM_001145410.1:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	NP_001138882.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
NM_007363.4:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	NP_031389.3:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
NM_007363.5:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG MANE Select	NP_031389.3:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
NM_001145408.2:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	NP_001138880.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
NM_001145409.2:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	NP_001138881.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG
NM_001145410.2:c.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG	NP_001138882.1:n.*28_*51delinsCCCTTAAAAGAAGGACCCTTTTTG