Canonical Allele Identifier: CA2694039270

Gene: NONO

Linked Data

• gnomAD v4: X-71300248-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300248A>G , CM000685.2:g.71300248A>G	GRCh38
NC_000023.10:g.70520098A>G , CM000685.1:g.70520098A>G	GRCh37
NC_000023.9:g.70436823A>G	NCBI36
NG_046742.1:g.22057A>G
NG_054891.1:g.3974A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*172A>G MANE Select	ENSP00000276079.8:n.*172A>G
ENST00000420903.6:c.*172A>G	ENSP00000410299.2:n.*172A>G
ENST00000473525.2:n.2296A>G
ENST00000676495.1:n.2999A>G
ENST00000676499.1:n.2544A>G
ENST00000676797.1:c.*172A>G	ENSP00000503920.1:n.*172A>G
ENST00000677014.1:c.*1415A>G	ENSP00000503813.1:n.*1415A>G
ENST00000677218.1:n.2759A>G
ENST00000677245.1:c.*1797A>G	ENSP00000503929.1:n.*1797A>G
ENST00000677274.1:c.*172A>G	ENSP00000504314.1:n.*172A>G
ENST00000677446.1:c.*172A>G	ENSP00000503031.1:n.*172A>G
ENST00000677612.1:c.*172A>G	ENSP00000504351.1:n.*172A>G
ENST00000677766.1:n.3993A>G
ENST00000677826.1:n.2330A>G
ENST00000677879.1:c.*172A>G	ENSP00000504090.1:n.*172A>G
ENST00000677977.1:n.3420A>G
ENST00000678231.1:c.*172A>G	ENSP00000503233.1:n.*172A>G
ENST00000678323.1:n.2686A>G
ENST00000678335.1:c.*501A>G	ENSP00000503769.1:n.*501A>G
ENST00000678437.1:c.*172A>G	ENSP00000504007.1:n.*172A>G
ENST00000678660.1:c.*172A>G	ENSP00000504665.1:n.*172A>G
ENST00000678830.1:c.*172A>G	ENSP00000504263.1:n.*172A>G
ENST00000679029.1:c.*402A>G	ENSP00000504193.1:n.*402A>G
ENST00000679267.1:n.3795A>G
ENST00000276079.12:c.*172A>G	ENSP00000276079.8:n.*172A>G
ENST00000373841.5:c.*172A>G	ENSP00000362947.1:n.*172A>G
ENST00000373856.7:c.*172A>G	ENSP00000362963.3:n.*172A>G
ENST00000472185.1:n.61-271A>G
ENST00000473525.1:n.1362A>G
ENST00000474431.5:n.623A>G
ENST00000490044.5:n.2295A>G
ENST00000535149.5:c.*172A>G	ENSP00000441364.1:n.*172A>G
NM_001145408.1:c.*172A>G	NP_001138880.1:n.*172A>G
NM_001145409.1:c.*172A>G	NP_001138881.1:n.*172A>G
NM_001145410.1:c.*172A>G	NP_001138882.1:n.*172A>G
NM_007363.4:c.*172A>G	NP_031389.3:n.*172A>G
NM_007363.5:c.*172A>G MANE Select	NP_031389.3:n.*172A>G
NM_001145408.2:c.*172A>G	NP_001138880.1:n.*172A>G
NM_001145409.2:c.*172A>G	NP_001138881.1:n.*172A>G
NM_001145410.2:c.*172A>G	NP_001138882.1:n.*172A>G