Canonical Allele Identifier: CA2694039273

Gene: NONO

Linked Data

• gnomAD v4: X-71300250-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300250_71300251insT , CM000685.2:g.71300250_71300251insT	GRCh38
NC_000023.10:g.70520100_70520101insT , CM000685.1:g.70520100_70520101insT	GRCh37
NC_000023.9:g.70436825_70436826insT	NCBI36
NG_046742.1:g.22059_22060insT
NG_054891.1:g.3976_3977insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*174_*175insT MANE Select	ENSP00000276079.8:n.*174_*175insT
ENST00000420903.6:c.*174_*175insT	ENSP00000410299.2:n.*174_*175insT
ENST00000473525.2:n.2298_2299insT
ENST00000676495.1:n.3001_3002insT
ENST00000676499.1:n.2546_2547insT
ENST00000676797.1:c.*174_*175insT	ENSP00000503920.1:n.*174_*175insT
ENST00000677014.1:c.*1417_*1418insT	ENSP00000503813.1:n.*1417_*1418insT
ENST00000677218.1:n.2761_2762insT
ENST00000677245.1:c.*1799_*1800insT	ENSP00000503929.1:n.*1799_*1800insT
ENST00000677274.1:c.*174_*175insT	ENSP00000504314.1:n.*174_*175insT
ENST00000677446.1:c.*174_*175insT	ENSP00000503031.1:n.*174_*175insT
ENST00000677612.1:c.*174_*175insT	ENSP00000504351.1:n.*174_*175insT
ENST00000677766.1:n.3995_3996insT
ENST00000677826.1:n.2332_2333insT
ENST00000677879.1:c.*174_*175insT	ENSP00000504090.1:n.*174_*175insT
ENST00000677977.1:n.3422_3423insT
ENST00000678231.1:c.*174_*175insT	ENSP00000503233.1:n.*174_*175insT
ENST00000678323.1:n.2688_2689insT
ENST00000678335.1:c.*503_*504insT	ENSP00000503769.1:n.*503_*504insT
ENST00000678437.1:c.*174_*175insT	ENSP00000504007.1:n.*174_*175insT
ENST00000678660.1:c.*174_*175insT	ENSP00000504665.1:n.*174_*175insT
ENST00000678830.1:c.*174_*175insT	ENSP00000504263.1:n.*174_*175insT
ENST00000679029.1:c.*404_*405insT	ENSP00000504193.1:n.*404_*405insT
ENST00000679267.1:n.3797_3798insT
ENST00000276079.12:c.*174_*175insT	ENSP00000276079.8:n.*174_*175insT
ENST00000373841.5:c.*174_*175insT	ENSP00000362947.1:n.*174_*175insT
ENST00000373856.7:c.*174_*175insT	ENSP00000362963.3:n.*174_*175insT
ENST00000472185.1:n.61-269_61-268insT
ENST00000473525.1:n.1364_1365insT
ENST00000474431.5:n.625_626insT
ENST00000490044.5:n.2297_2298insT
ENST00000535149.5:c.*174_*175insT	ENSP00000441364.1:n.*174_*175insT
NM_001145408.1:c.*174_*175insT	NP_001138880.1:n.*174_*175insT
NM_001145409.1:c.*174_*175insT	NP_001138881.1:n.*174_*175insT
NM_001145410.1:c.*174_*175insT	NP_001138882.1:n.*174_*175insT
NM_007363.4:c.*174_*175insT	NP_031389.3:n.*174_*175insT
NM_007363.5:c.*174_*175insT MANE Select	NP_031389.3:n.*174_*175insT
NM_001145408.2:c.*174_*175insT	NP_001138880.1:n.*174_*175insT
NM_001145409.2:c.*174_*175insT	NP_001138881.1:n.*174_*175insT
NM_001145410.2:c.*174_*175insT	NP_001138882.1:n.*174_*175insT