Canonical Allele Identifier: CA2694039267

Gene: NONO

Linked Data

• gnomAD v4: X-71300242-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300242G>T , CM000685.2:g.71300242G>T	GRCh38
NC_000023.10:g.70520092G>T , CM000685.1:g.70520092G>T	GRCh37
NC_000023.9:g.70436817G>T	NCBI36
NG_046742.1:g.22051G>T
NG_054891.1:g.3968G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*166G>T MANE Select	ENSP00000276079.8:n.*166G>T
ENST00000420903.6:c.*166G>T	ENSP00000410299.2:n.*166G>T
ENST00000473525.2:n.2290G>T
ENST00000676495.1:n.2993G>T
ENST00000676499.1:n.2538G>T
ENST00000676797.1:c.*166G>T	ENSP00000503920.1:n.*166G>T
ENST00000677014.1:c.*1409G>T	ENSP00000503813.1:n.*1409G>T
ENST00000677218.1:n.2753G>T
ENST00000677245.1:c.*1791G>T	ENSP00000503929.1:n.*1791G>T
ENST00000677274.1:c.*166G>T	ENSP00000504314.1:n.*166G>T
ENST00000677446.1:c.*166G>T	ENSP00000503031.1:n.*166G>T
ENST00000677612.1:c.*166G>T	ENSP00000504351.1:n.*166G>T
ENST00000677766.1:n.3987G>T
ENST00000677826.1:n.2324G>T
ENST00000677879.1:c.*166G>T	ENSP00000504090.1:n.*166G>T
ENST00000677977.1:n.3414G>T
ENST00000678231.1:c.*166G>T	ENSP00000503233.1:n.*166G>T
ENST00000678323.1:n.2680G>T
ENST00000678335.1:c.*495G>T	ENSP00000503769.1:n.*495G>T
ENST00000678437.1:c.*166G>T	ENSP00000504007.1:n.*166G>T
ENST00000678660.1:c.*166G>T	ENSP00000504665.1:n.*166G>T
ENST00000678830.1:c.*166G>T	ENSP00000504263.1:n.*166G>T
ENST00000679029.1:c.*396G>T	ENSP00000504193.1:n.*396G>T
ENST00000679267.1:n.3789G>T
ENST00000276079.12:c.*166G>T	ENSP00000276079.8:n.*166G>T
ENST00000373841.5:c.*166G>T	ENSP00000362947.1:n.*166G>T
ENST00000373856.7:c.*166G>T	ENSP00000362963.3:n.*166G>T
ENST00000472185.1:n.61-277G>T
ENST00000473525.1:n.1356G>T
ENST00000474431.5:n.617G>T
ENST00000490044.5:n.2289G>T
ENST00000535149.5:c.*166G>T	ENSP00000441364.1:n.*166G>T
NM_001145408.1:c.*166G>T	NP_001138880.1:n.*166G>T
NM_001145409.1:c.*166G>T	NP_001138881.1:n.*166G>T
NM_001145410.1:c.*166G>T	NP_001138882.1:n.*166G>T
NM_007363.4:c.*166G>T	NP_031389.3:n.*166G>T
NM_007363.5:c.*166G>T MANE Select	NP_031389.3:n.*166G>T
NM_001145408.2:c.*166G>T	NP_001138880.1:n.*166G>T
NM_001145409.2:c.*166G>T	NP_001138881.1:n.*166G>T
NM_001145410.2:c.*166G>T	NP_001138882.1:n.*166G>T