Canonical Allele Identifier: CA413549898

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519792A>T (hg19) ; chrX:g.71299942A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299942A>T , CM000685.2:g.71299942A>T	GRCh38
NC_000023.10:g.70519792A>T , CM000685.1:g.70519792A>T	GRCh37
NC_000023.9:g.70436517A>T	NCBI36
NG_046742.1:g.21751A>T
NG_054891.1:g.3668A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1282A>T MANE Select	ENSP00000276079.8:p.Thr428Ser
ENST00000373856.8:c.1380A>T	ENSP00000362963.4:p.Arg460Ser
ENST00000420903.6:c.1282A>T	ENSP00000410299.2:p.Thr428Ser
ENST00000450092.6:c.1282A>T	ENSP00000415777.2:p.Thr428Ser
ENST00000454976.2:c.1282A>T	ENSP00000406673.2:p.Thr428Ser
ENST00000473525.2:n.1990A>T
ENST00000676495.1:n.2693A>T
ENST00000676499.1:n.2238A>T
ENST00000676797.1:c.1015A>T	ENSP00000503920.1:p.Thr339Ser
ENST00000677014.1:c.*1109A>T	ENSP00000503813.1:n.*1109A>T
ENST00000677218.1:n.2453A>T
ENST00000677245.1:c.*1491A>T	ENSP00000503929.1:n.*1491A>T
ENST00000677274.1:c.1282A>T	ENSP00000504314.1:p.Thr428Ser
ENST00000677446.1:c.1282A>T	ENSP00000503031.1:p.Thr428Ser
ENST00000677612.1:c.1282A>T	ENSP00000504351.1:p.Thr428Ser
ENST00000677766.1:n.3687A>T
ENST00000677826.1:n.2024A>T
ENST00000677879.1:c.1102A>T	ENSP00000504090.1:p.Thr368Ser
ENST00000677977.1:n.3114A>T
ENST00000678231.1:c.1282A>T	ENSP00000503233.1:p.Thr428Ser
ENST00000678323.1:n.2380A>T
ENST00000678335.1:c.*195A>T	ENSP00000503769.1:n.*195A>T
ENST00000678437.1:c.1273A>T	ENSP00000504007.1:p.Thr425Ser
ENST00000678660.1:c.1297A>T	ENSP00000504665.1:p.Thr433Ser
ENST00000678830.1:c.1372A>T	ENSP00000504263.1:p.Thr458Ser
ENST00000679029.1:c.*96A>T	ENSP00000504193.1:n.*96A>T
ENST00000679267.1:n.3489A>T
ENST00000276079.12:c.1282A>T	ENSP00000276079.8:p.Thr428Ser
ENST00000373841.5:c.1282A>T	ENSP00000362947.1:p.Thr428Ser
ENST00000373856.7:c.1282A>T	ENSP00000362963.3:p.Thr428Ser
ENST00000472185.1:n.61-577A>T
ENST00000473525.1:n.1056A>T
ENST00000474431.5:n.317A>T
ENST00000490044.5:n.1989A>T
ENST00000535149.5:c.1015A>T	ENSP00000441364.1:p.Thr339Ser
NM_001145408.1:c.1282A>T	NP_001138880.1:p.Thr428Ser
NM_001145409.1:c.1282A>T	NP_001138881.1:p.Thr428Ser
NM_001145410.1:c.1015A>T	NP_001138882.1:p.Thr339Ser
NM_007363.4:c.1282A>T	NP_031389.3:p.Thr428Ser
NM_007363.5:c.1282A>T MANE Select	NP_031389.3:p.Thr428Ser
NM_001145408.2:c.1282A>T	NP_001138880.1:p.Thr428Ser
NM_001145409.2:c.1282A>T	NP_001138881.1:p.Thr428Ser
NM_001145410.2:c.1015A>T	NP_001138882.1:p.Thr339Ser