Canonical Allele Identifier: CA2539399287

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300080G>A , CM000685.2:g.71300080G>A	GRCh38
NC_000023.10:g.70519930G>A , CM000685.1:g.70519930G>A	GRCh37
NC_000023.9:g.70436655G>A	NCBI36
NG_046742.1:g.21889G>A
NG_054891.1:g.3806G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*4G>A MANE Select	ENSP00000276079.8:n.*4G>A
ENST00000373856.8:c.1518G>A	ENSP00000362963.4:p.Lys506=
ENST00000420903.6:c.*4G>A	ENSP00000410299.2:n.*4G>A
ENST00000473525.2:n.2128G>A
ENST00000676495.1:n.2831G>A
ENST00000676499.1:n.2376G>A
ENST00000676797.1:c.*4G>A	ENSP00000503920.1:n.*4G>A
ENST00000677014.1:c.*1247G>A	ENSP00000503813.1:n.*1247G>A
ENST00000677218.1:n.2591G>A
ENST00000677245.1:c.*1629G>A	ENSP00000503929.1:n.*1629G>A
ENST00000677274.1:c.*4G>A	ENSP00000504314.1:n.*4G>A
ENST00000677446.1:c.*4G>A	ENSP00000503031.1:n.*4G>A
ENST00000677612.1:c.*4G>A	ENSP00000504351.1:n.*4G>A
ENST00000677766.1:n.3825G>A
ENST00000677826.1:n.2162G>A
ENST00000677879.1:c.*4G>A	ENSP00000504090.1:n.*4G>A
ENST00000677977.1:n.3252G>A
ENST00000678231.1:c.*4G>A	ENSP00000503233.1:n.*4G>A
ENST00000678323.1:n.2518G>A
ENST00000678335.1:c.*333G>A	ENSP00000503769.1:n.*333G>A
ENST00000678437.1:c.*4G>A	ENSP00000504007.1:n.*4G>A
ENST00000678660.1:c.*4G>A	ENSP00000504665.1:n.*4G>A
ENST00000678830.1:c.*4G>A	ENSP00000504263.1:n.*4G>A
ENST00000679029.1:c.*234G>A	ENSP00000504193.1:n.*234G>A
ENST00000679267.1:n.3627G>A
ENST00000276079.12:c.*4G>A	ENSP00000276079.8:n.*4G>A
ENST00000373841.5:c.*4G>A	ENSP00000362947.1:n.*4G>A
ENST00000373856.7:c.*4G>A	ENSP00000362963.3:n.*4G>A
ENST00000472185.1:n.61-439G>A
ENST00000473525.1:n.1194G>A
ENST00000474431.5:n.455G>A
ENST00000490044.5:n.2127G>A
ENST00000535149.5:c.*4G>A	ENSP00000441364.1:n.*4G>A
NM_001145408.1:c.*4G>A	NP_001138880.1:n.*4G>A
NM_001145409.1:c.*4G>A	NP_001138881.1:n.*4G>A
NM_001145410.1:c.*4G>A	NP_001138882.1:n.*4G>A
NM_007363.4:c.*4G>A	NP_031389.3:n.*4G>A
NM_007363.5:c.*4G>A MANE Select	NP_031389.3:n.*4G>A
NM_001145408.2:c.*4G>A	NP_001138880.1:n.*4G>A
NM_001145409.2:c.*4G>A	NP_001138881.1:n.*4G>A
NM_001145410.2:c.*4G>A	NP_001138882.1:n.*4G>A