Canonical Allele Identifier: CA413550031

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519811G>A (hg19) ; chrX:g.71299961G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299961G>A , CM000685.2:g.71299961G>A	GRCh38
NC_000023.10:g.70519811G>A , CM000685.1:g.70519811G>A	GRCh37
NC_000023.9:g.70436536G>A	NCBI36
NG_046742.1:g.21770G>A
NG_054891.1:g.3687G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000276079.13:c.1301G>A MANE Select	ENSP00000276079.8:p.Arg434His
ENST00000373856.8:c.1399G>A	ENSP00000362963.4:p.Ala467Thr
ENST00000420903.6:c.1301G>A	ENSP00000410299.2:p.Arg434His
ENST00000450092.6:c.1301G>A	ENSP00000415777.2:p.Arg434His
ENST00000454976.2:c.1301G>A	ENSP00000406673.2:p.Arg434His
ENST00000473525.2:n.2009G>A
ENST00000676495.1:n.2712G>A
ENST00000676499.1:n.2257G>A
ENST00000676797.1:c.1034G>A	ENSP00000503920.1:p.Arg345His
ENST00000677014.1:c.*1128G>A	ENSP00000503813.1:n.*1128G>A
ENST00000677218.1:n.2472G>A
ENST00000677245.1:c.*1510G>A	ENSP00000503929.1:n.*1510G>A
ENST00000677274.1:c.1301G>A	ENSP00000504314.1:p.Arg434His
ENST00000677446.1:c.1301G>A	ENSP00000503031.1:p.Arg434His
ENST00000677612.1:c.1301G>A	ENSP00000504351.1:p.Arg434His
ENST00000677766.1:n.3706G>A
ENST00000677826.1:n.2043G>A
ENST00000677879.1:c.1121G>A	ENSP00000504090.1:p.Arg374His
ENST00000677977.1:n.3133G>A
ENST00000678231.1:c.1301G>A	ENSP00000503233.1:p.Arg434His
ENST00000678323.1:n.2399G>A
ENST00000678335.1:c.*214G>A	ENSP00000503769.1:n.*214G>A
ENST00000678437.1:c.1292G>A	ENSP00000504007.1:p.Arg431His
ENST00000678660.1:c.1316G>A	ENSP00000504665.1:p.Arg439His
ENST00000678830.1:c.1391G>A	ENSP00000504263.1:p.Arg464His
ENST00000679029.1:c.*115G>A	ENSP00000504193.1:n.*115G>A
ENST00000679267.1:n.3508G>A
ENST00000276079.12:c.1301G>A	ENSP00000276079.8:p.Arg434His
ENST00000373841.5:c.1301G>A	ENSP00000362947.1:p.Arg434His
ENST00000373856.7:c.1301G>A	ENSP00000362963.3:p.Arg434His
ENST00000472185.1:n.61-558G>A
ENST00000473525.1:n.1075G>A
ENST00000474431.5:n.336G>A
ENST00000490044.5:n.2008G>A
ENST00000535149.5:c.1034G>A	ENSP00000441364.1:p.Arg345His
NM_001145408.1:c.1301G>A	NP_001138880.1:p.Arg434His
NM_001145409.1:c.1301G>A	NP_001138881.1:p.Arg434His
NM_001145410.1:c.1034G>A	NP_001138882.1:p.Arg345His
NM_007363.4:c.1301G>A	NP_031389.3:p.Arg434His
NM_007363.5:c.1301G>A MANE Select	NP_031389.3:p.Arg434His
NM_001145408.2:c.1301G>A	NP_001138880.1:p.Arg434His
NM_001145409.2:c.1301G>A	NP_001138881.1:p.Arg434His
NM_001145410.2:c.1034G>A	NP_001138882.1:p.Arg345His