Canonical Allele Identifier: CA413550585

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519898T>A (hg19) ; chrX:g.71300048T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300048T>A , CM000685.2:g.71300048T>A	GRCh38
NC_000023.10:g.70519898T>A , CM000685.1:g.70519898T>A	GRCh37
NC_000023.9:g.70436623T>A	NCBI36
NG_046742.1:g.21857T>A
NG_054891.1:g.3774T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1388T>A MANE Select	ENSP00000276079.8:p.Phe463Tyr
ENST00000373856.8:c.1486T>A	ENSP00000362963.4:p.Leu496Met
ENST00000420903.6:c.1388T>A	ENSP00000410299.2:p.Phe463Tyr
ENST00000450092.6:c.1388T>A	ENSP00000415777.2:p.Phe463Tyr
ENST00000454976.2:c.1388T>A	ENSP00000406673.2:p.Phe463Tyr
ENST00000473525.2:n.2096T>A
ENST00000676495.1:n.2799T>A
ENST00000676499.1:n.2344T>A
ENST00000676797.1:c.1121T>A	ENSP00000503920.1:p.Phe374Tyr
ENST00000677014.1:c.*1215T>A	ENSP00000503813.1:n.*1215T>A
ENST00000677218.1:n.2559T>A
ENST00000677245.1:c.*1597T>A	ENSP00000503929.1:n.*1597T>A
ENST00000677274.1:c.1388T>A	ENSP00000504314.1:p.Phe463Tyr
ENST00000677446.1:c.1388T>A	ENSP00000503031.1:p.Phe463Tyr
ENST00000677612.1:c.1388T>A	ENSP00000504351.1:p.Phe463Tyr
ENST00000677766.1:n.3793T>A
ENST00000677826.1:n.2130T>A
ENST00000677879.1:c.1208T>A	ENSP00000504090.1:p.Phe403Tyr
ENST00000677977.1:n.3220T>A
ENST00000678231.1:c.1388T>A	ENSP00000503233.1:p.Phe463Tyr
ENST00000678323.1:n.2486T>A
ENST00000678335.1:c.*301T>A	ENSP00000503769.1:n.*301T>A
ENST00000678437.1:c.1379T>A	ENSP00000504007.1:p.Phe460Tyr
ENST00000678660.1:c.1403T>A	ENSP00000504665.1:p.Phe468Tyr
ENST00000678830.1:c.1478T>A	ENSP00000504263.1:p.Phe493Tyr
ENST00000679029.1:c.*202T>A	ENSP00000504193.1:n.*202T>A
ENST00000679267.1:n.3595T>A
ENST00000276079.12:c.1388T>A	ENSP00000276079.8:p.Phe463Tyr
ENST00000373841.5:c.1388T>A	ENSP00000362947.1:p.Phe463Tyr
ENST00000373856.7:c.1388T>A	ENSP00000362963.3:p.Phe463Tyr
ENST00000472185.1:n.61-471T>A
ENST00000473525.1:n.1162T>A
ENST00000474431.5:n.423T>A
ENST00000490044.5:n.2095T>A
ENST00000535149.5:c.1121T>A	ENSP00000441364.1:p.Phe374Tyr
NM_001145408.1:c.1388T>A	NP_001138880.1:p.Phe463Tyr
NM_001145409.1:c.1388T>A	NP_001138881.1:p.Phe463Tyr
NM_001145410.1:c.1121T>A	NP_001138882.1:p.Phe374Tyr
NM_007363.4:c.1388T>A	NP_031389.3:p.Phe463Tyr
NM_007363.5:c.1388T>A MANE Select	NP_031389.3:p.Phe463Tyr
NM_001145408.2:c.1388T>A	NP_001138880.1:p.Phe463Tyr
NM_001145409.2:c.1388T>A	NP_001138881.1:p.Phe463Tyr
NM_001145410.2:c.1121T>A	NP_001138882.1:p.Phe374Tyr