Canonical Allele Identifier: CA516732272

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519803A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299953A>G , CM000685.2:g.71299953A>G	GRCh38
NC_000023.10:g.70519803A>G , CM000685.1:g.70519803A>G	GRCh37
NC_000023.9:g.70436528A>G	NCBI36
NG_046742.1:g.21762A>G
NG_054891.1:g.3679A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000276079.13:c.1293A>G MANE Select	ENSP00000276079.8:p.Thr431=
ENST00000373856.8:c.1391A>G	ENSP00000362963.4:p.Gln464Arg
ENST00000420903.6:c.1293A>G	ENSP00000410299.2:p.Thr431=
ENST00000450092.6:c.1293A>G	ENSP00000415777.2:p.Thr431=
ENST00000454976.2:c.1293A>G	ENSP00000406673.2:p.Thr431=
ENST00000473525.2:n.2001A>G
ENST00000676495.1:n.2704A>G
ENST00000676499.1:n.2249A>G
ENST00000676797.1:c.1026A>G	ENSP00000503920.1:p.Thr342=
ENST00000677014.1:c.*1120A>G	ENSP00000503813.1:n.*1120A>G
ENST00000677218.1:n.2464A>G
ENST00000677245.1:c.*1502A>G	ENSP00000503929.1:n.*1502A>G
ENST00000677274.1:c.1293A>G	ENSP00000504314.1:p.Thr431=
ENST00000677446.1:c.1293A>G	ENSP00000503031.1:p.Thr431=
ENST00000677612.1:c.1293A>G	ENSP00000504351.1:p.Thr431=
ENST00000677766.1:n.3698A>G
ENST00000677826.1:n.2035A>G
ENST00000677879.1:c.1113A>G	ENSP00000504090.1:p.Thr371=
ENST00000677977.1:n.3125A>G
ENST00000678231.1:c.1293A>G	ENSP00000503233.1:p.Thr431=
ENST00000678323.1:n.2391A>G
ENST00000678335.1:c.*206A>G	ENSP00000503769.1:n.*206A>G
ENST00000678437.1:c.1284A>G	ENSP00000504007.1:p.Thr428=
ENST00000678660.1:c.1308A>G	ENSP00000504665.1:p.Thr436=
ENST00000678830.1:c.1383A>G	ENSP00000504263.1:p.Thr461=
ENST00000679029.1:c.*107A>G	ENSP00000504193.1:n.*107A>G
ENST00000679267.1:n.3500A>G
ENST00000276079.12:c.1293A>G	ENSP00000276079.8:p.Thr431=
ENST00000373841.5:c.1293A>G	ENSP00000362947.1:p.Thr431=
ENST00000373856.7:c.1293A>G	ENSP00000362963.3:p.Thr431=
ENST00000472185.1:n.61-566A>G
ENST00000473525.1:n.1067A>G
ENST00000474431.5:n.328A>G
ENST00000490044.5:n.2000A>G
ENST00000535149.5:c.1026A>G	ENSP00000441364.1:p.Thr342=
NM_001145408.1:c.1293A>G	NP_001138880.1:p.Thr431=
NM_001145409.1:c.1293A>G	NP_001138881.1:p.Thr431=
NM_001145410.1:c.1026A>G	NP_001138882.1:p.Thr342=
NM_007363.4:c.1293A>G	NP_031389.3:p.Thr431=
NM_007363.5:c.1293A>G MANE Select	NP_031389.3:p.Thr431=
NM_001145408.2:c.1293A>G	NP_001138880.1:p.Thr431=
NM_001145409.2:c.1293A>G	NP_001138881.1:p.Thr431=
NM_001145410.2:c.1026A>G	NP_001138882.1:p.Thr342=