Canonical Allele Identifier: CA2694039262

Gene: NONO

Linked Data

• gnomAD v4: X-71300236-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300236G>T , CM000685.2:g.71300236G>T	GRCh38
NC_000023.10:g.70520086G>T , CM000685.1:g.70520086G>T	GRCh37
NC_000023.9:g.70436811G>T	NCBI36
NG_046742.1:g.22045G>T
NG_054891.1:g.3962G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*160G>T MANE Select	ENSP00000276079.8:n.*160G>T
ENST00000420903.6:c.*160G>T	ENSP00000410299.2:n.*160G>T
ENST00000473525.2:n.2284G>T
ENST00000676495.1:n.2987G>T
ENST00000676499.1:n.2532G>T
ENST00000676797.1:c.*160G>T	ENSP00000503920.1:n.*160G>T
ENST00000677014.1:c.*1403G>T	ENSP00000503813.1:n.*1403G>T
ENST00000677218.1:n.2747G>T
ENST00000677245.1:c.*1785G>T	ENSP00000503929.1:n.*1785G>T
ENST00000677274.1:c.*160G>T	ENSP00000504314.1:n.*160G>T
ENST00000677446.1:c.*160G>T	ENSP00000503031.1:n.*160G>T
ENST00000677612.1:c.*160G>T	ENSP00000504351.1:n.*160G>T
ENST00000677766.1:n.3981G>T
ENST00000677826.1:n.2318G>T
ENST00000677879.1:c.*160G>T	ENSP00000504090.1:n.*160G>T
ENST00000677977.1:n.3408G>T
ENST00000678231.1:c.*160G>T	ENSP00000503233.1:n.*160G>T
ENST00000678323.1:n.2674G>T
ENST00000678335.1:c.*489G>T	ENSP00000503769.1:n.*489G>T
ENST00000678437.1:c.*160G>T	ENSP00000504007.1:n.*160G>T
ENST00000678660.1:c.*160G>T	ENSP00000504665.1:n.*160G>T
ENST00000678830.1:c.*160G>T	ENSP00000504263.1:n.*160G>T
ENST00000679029.1:c.*390G>T	ENSP00000504193.1:n.*390G>T
ENST00000679267.1:n.3783G>T
ENST00000276079.12:c.*160G>T	ENSP00000276079.8:n.*160G>T
ENST00000373841.5:c.*160G>T	ENSP00000362947.1:n.*160G>T
ENST00000373856.7:c.*160G>T	ENSP00000362963.3:n.*160G>T
ENST00000472185.1:n.61-283G>T
ENST00000473525.1:n.1350G>T
ENST00000474431.5:n.611G>T
ENST00000490044.5:n.2283G>T
ENST00000535149.5:c.*160G>T	ENSP00000441364.1:n.*160G>T
NM_001145408.1:c.*160G>T	NP_001138880.1:n.*160G>T
NM_001145409.1:c.*160G>T	NP_001138881.1:n.*160G>T
NM_001145410.1:c.*160G>T	NP_001138882.1:n.*160G>T
NM_007363.4:c.*160G>T	NP_031389.3:n.*160G>T
NM_007363.5:c.*160G>T MANE Select	NP_031389.3:n.*160G>T
NM_001145408.2:c.*160G>T	NP_001138880.1:n.*160G>T
NM_001145409.2:c.*160G>T	NP_001138881.1:n.*160G>T
NM_001145410.2:c.*160G>T	NP_001138882.1:n.*160G>T