Canonical Allele Identifier: CA2436414858

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299971G= , CM000685.2:g.71299971G=	GRCh38
NC_000023.10:g.70519821G= , CM000685.1:g.70519821G=	GRCh37
NC_000023.9:g.70436546G=	NCBI36
NG_046742.1:g.21780G=
NG_054891.1:g.3697G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1311G= MANE Select	ENSP00000276079.8:p.Gln437=
ENST00000373856.8:c.1409G=	ENSP00000362963.4:p.Arg470=
ENST00000420903.6:c.1311G=	ENSP00000410299.2:p.Gln437=
ENST00000450092.6:c.1311G=	ENSP00000415777.2:p.Gln437=
ENST00000454976.2:c.1311G=	ENSP00000406673.2:p.Gln437=
ENST00000473525.2:n.2019G=
ENST00000676495.1:n.2722G=
ENST00000676499.1:n.2267G=
ENST00000676797.1:c.1044G=	ENSP00000503920.1:p.Gln348=
ENST00000677014.1:c.*1138G=	ENSP00000503813.1:n.*1138G=
ENST00000677218.1:n.2482G=
ENST00000677245.1:c.*1520G=	ENSP00000503929.1:n.*1520G=
ENST00000677274.1:c.1311G=	ENSP00000504314.1:p.Gln437=
ENST00000677446.1:c.1311G=	ENSP00000503031.1:p.Gln437=
ENST00000677612.1:c.1311G=	ENSP00000504351.1:p.Gln437=
ENST00000677766.1:n.3716G=
ENST00000677826.1:n.2053G=
ENST00000677879.1:c.1131G=	ENSP00000504090.1:p.Gln377=
ENST00000677977.1:n.3143G=
ENST00000678231.1:c.1311G=	ENSP00000503233.1:p.Gln437=
ENST00000678323.1:n.2409G=
ENST00000678335.1:c.*224G=	ENSP00000503769.1:n.*224G=
ENST00000678437.1:c.1302G=	ENSP00000504007.1:p.Gln434=
ENST00000678660.1:c.1326G=	ENSP00000504665.1:p.Gln442=
ENST00000678830.1:c.1401G=	ENSP00000504263.1:p.Gln467=
ENST00000679029.1:c.*125G=	ENSP00000504193.1:n.*125G=
ENST00000679267.1:n.3518G=
ENST00000276079.12:c.1311G=	ENSP00000276079.8:p.Gln437=
ENST00000373841.5:c.1311G=	ENSP00000362947.1:p.Gln437=
ENST00000373856.7:c.1311G=	ENSP00000362963.3:p.Gln437=
ENST00000472185.1:n.61-548G=
ENST00000473525.1:n.1085G=
ENST00000474431.5:n.346G=
ENST00000490044.5:n.2018G=
ENST00000535149.5:c.1044G=	ENSP00000441364.1:p.Gln348=
NM_001145408.1:c.1311G=	NP_001138880.1:p.Gln437=
NM_001145409.1:c.1311G=	NP_001138881.1:p.Gln437=
NM_001145410.1:c.1044G=	NP_001138882.1:p.Gln348=
NM_007363.4:c.1311G=	NP_031389.3:p.Gln437=
NM_007363.5:c.1311G= MANE Select	NP_031389.3:p.Gln437=
NM_001145408.2:c.1311G=	NP_001138880.1:p.Gln437=
NM_001145409.2:c.1311G=	NP_001138881.1:p.Gln437=
NM_001145410.2:c.1044G=	NP_001138882.1:p.Gln348=