Canonical Allele Identifier: CA2436414864

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299996G= , CM000685.2:g.71299996G=	GRCh38
NC_000023.10:g.70519846G= , CM000685.1:g.70519846G=	GRCh37
NC_000023.9:g.70436571G=	NCBI36
NG_046742.1:g.21805G=
NG_054891.1:g.3722G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1336G= MANE Select	ENSP00000276079.8:p.Ala446=
ENST00000373856.8:c.1434G=	ENSP00000362963.4:p.Gly478=
ENST00000420903.6:c.1336G=	ENSP00000410299.2:p.Ala446=
ENST00000450092.6:c.1336G=	ENSP00000415777.2:p.Ala446=
ENST00000454976.2:c.1336G=	ENSP00000406673.2:p.Ala446=
ENST00000473525.2:n.2044G=
ENST00000676495.1:n.2747G=
ENST00000676499.1:n.2292G=
ENST00000676797.1:c.1069G=	ENSP00000503920.1:p.Ala357=
ENST00000677014.1:c.*1163G=	ENSP00000503813.1:n.*1163G=
ENST00000677218.1:n.2507G=
ENST00000677245.1:c.*1545G=	ENSP00000503929.1:n.*1545G=
ENST00000677274.1:c.1336G=	ENSP00000504314.1:p.Ala446=
ENST00000677446.1:c.1336G=	ENSP00000503031.1:p.Ala446=
ENST00000677612.1:c.1336G=	ENSP00000504351.1:p.Ala446=
ENST00000677766.1:n.3741G=
ENST00000677826.1:n.2078G=
ENST00000677879.1:c.1156G=	ENSP00000504090.1:p.Ala386=
ENST00000677977.1:n.3168G=
ENST00000678231.1:c.1336G=	ENSP00000503233.1:p.Ala446=
ENST00000678323.1:n.2434G=
ENST00000678335.1:c.*249G=	ENSP00000503769.1:n.*249G=
ENST00000678437.1:c.1327G=	ENSP00000504007.1:p.Ala443=
ENST00000678660.1:c.1351G=	ENSP00000504665.1:p.Ala451=
ENST00000678830.1:c.1426G=	ENSP00000504263.1:p.Ala476=
ENST00000679029.1:c.*150G=	ENSP00000504193.1:n.*150G=
ENST00000679267.1:n.3543G=
ENST00000276079.12:c.1336G=	ENSP00000276079.8:p.Ala446=
ENST00000373841.5:c.1336G=	ENSP00000362947.1:p.Ala446=
ENST00000373856.7:c.1336G=	ENSP00000362963.3:p.Ala446=
ENST00000472185.1:n.61-523G=
ENST00000473525.1:n.1110G=
ENST00000474431.5:n.371G=
ENST00000490044.5:n.2043G=
ENST00000535149.5:c.1069G=	ENSP00000441364.1:p.Ala357=
NM_001145408.1:c.1336G=	NP_001138880.1:p.Ala446=
NM_001145409.1:c.1336G=	NP_001138881.1:p.Ala446=
NM_001145410.1:c.1069G=	NP_001138882.1:p.Ala357=
NM_007363.4:c.1336G=	NP_031389.3:p.Ala446=
NM_007363.5:c.1336G= MANE Select	NP_031389.3:p.Ala446=
NM_001145408.2:c.1336G=	NP_001138880.1:p.Ala446=
NM_001145409.2:c.1336G=	NP_001138881.1:p.Ala446=
NM_001145410.2:c.1069G=	NP_001138882.1:p.Ala357=