Canonical Allele Identifier: CA413549947

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519798C>A (hg19) ; chrX:g.71299948C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299948C>A , CM000685.2:g.71299948C>A	GRCh38
NC_000023.10:g.70519798C>A , CM000685.1:g.70519798C>A	GRCh37
NC_000023.9:g.70436523C>A	NCBI36
NG_046742.1:g.21757C>A
NG_054891.1:g.3674C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1288C>A MANE Select	ENSP00000276079.8:p.Pro430Thr
ENST00000373856.8:c.1386C>A	ENSP00000362963.4:p.His462Gln
ENST00000420903.6:c.1288C>A	ENSP00000410299.2:p.Pro430Thr
ENST00000450092.6:c.1288C>A	ENSP00000415777.2:p.Pro430Thr
ENST00000454976.2:c.1288C>A	ENSP00000406673.2:p.Pro430Thr
ENST00000473525.2:n.1996C>A
ENST00000676495.1:n.2699C>A
ENST00000676499.1:n.2244C>A
ENST00000676797.1:c.1021C>A	ENSP00000503920.1:p.Pro341Thr
ENST00000677014.1:c.*1115C>A	ENSP00000503813.1:n.*1115C>A
ENST00000677218.1:n.2459C>A
ENST00000677245.1:c.*1497C>A	ENSP00000503929.1:n.*1497C>A
ENST00000677274.1:c.1288C>A	ENSP00000504314.1:p.Pro430Thr
ENST00000677446.1:c.1288C>A	ENSP00000503031.1:p.Pro430Thr
ENST00000677612.1:c.1288C>A	ENSP00000504351.1:p.Pro430Thr
ENST00000677766.1:n.3693C>A
ENST00000677826.1:n.2030C>A
ENST00000677879.1:c.1108C>A	ENSP00000504090.1:p.Pro370Thr
ENST00000677977.1:n.3120C>A
ENST00000678231.1:c.1288C>A	ENSP00000503233.1:p.Pro430Thr
ENST00000678323.1:n.2386C>A
ENST00000678335.1:c.*201C>A	ENSP00000503769.1:n.*201C>A
ENST00000678437.1:c.1279C>A	ENSP00000504007.1:p.Pro427Thr
ENST00000678660.1:c.1303C>A	ENSP00000504665.1:p.Pro435Thr
ENST00000678830.1:c.1378C>A	ENSP00000504263.1:p.Pro460Thr
ENST00000679029.1:c.*102C>A	ENSP00000504193.1:n.*102C>A
ENST00000679267.1:n.3495C>A
ENST00000276079.12:c.1288C>A	ENSP00000276079.8:p.Pro430Thr
ENST00000373841.5:c.1288C>A	ENSP00000362947.1:p.Pro430Thr
ENST00000373856.7:c.1288C>A	ENSP00000362963.3:p.Pro430Thr
ENST00000472185.1:n.61-571C>A
ENST00000473525.1:n.1062C>A
ENST00000474431.5:n.323C>A
ENST00000490044.5:n.1995C>A
ENST00000535149.5:c.1021C>A	ENSP00000441364.1:p.Pro341Thr
NM_001145408.1:c.1288C>A	NP_001138880.1:p.Pro430Thr
NM_001145409.1:c.1288C>A	NP_001138881.1:p.Pro430Thr
NM_001145410.1:c.1021C>A	NP_001138882.1:p.Pro341Thr
NM_007363.4:c.1288C>A	NP_031389.3:p.Pro430Thr
NM_007363.5:c.1288C>A MANE Select	NP_031389.3:p.Pro430Thr
NM_001145408.2:c.1288C>A	NP_001138880.1:p.Pro430Thr
NM_001145409.2:c.1288C>A	NP_001138881.1:p.Pro430Thr
NM_001145410.2:c.1021C>A	NP_001138882.1:p.Pro341Thr