Canonical Allele Identifier: CA2436414859

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299972G= , CM000685.2:g.71299972G=	GRCh38
NC_000023.10:g.70519822G= , CM000685.1:g.70519822G=	GRCh37
NC_000023.9:g.70436547G=	NCBI36
NG_046742.1:g.21781G=
NG_054891.1:g.3698G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1312G= MANE Select	ENSP00000276079.8:p.Ala438=
ENST00000373856.8:c.1410G=	ENSP00000362963.4:p.Arg470=
ENST00000420903.6:c.1312G=	ENSP00000410299.2:p.Ala438=
ENST00000450092.6:c.1312G=	ENSP00000415777.2:p.Ala438=
ENST00000454976.2:c.1312G=	ENSP00000406673.2:p.Ala438=
ENST00000473525.2:n.2020G=
ENST00000676495.1:n.2723G=
ENST00000676499.1:n.2268G=
ENST00000676797.1:c.1045G=	ENSP00000503920.1:p.Ala349=
ENST00000677014.1:c.*1139G=	ENSP00000503813.1:n.*1139G=
ENST00000677218.1:n.2483G=
ENST00000677245.1:c.*1521G=	ENSP00000503929.1:n.*1521G=
ENST00000677274.1:c.1312G=	ENSP00000504314.1:p.Ala438=
ENST00000677446.1:c.1312G=	ENSP00000503031.1:p.Ala438=
ENST00000677612.1:c.1312G=	ENSP00000504351.1:p.Ala438=
ENST00000677766.1:n.3717G=
ENST00000677826.1:n.2054G=
ENST00000677879.1:c.1132G=	ENSP00000504090.1:p.Ala378=
ENST00000677977.1:n.3144G=
ENST00000678231.1:c.1312G=	ENSP00000503233.1:p.Ala438=
ENST00000678323.1:n.2410G=
ENST00000678335.1:c.*225G=	ENSP00000503769.1:n.*225G=
ENST00000678437.1:c.1303G=	ENSP00000504007.1:p.Ala435=
ENST00000678660.1:c.1327G=	ENSP00000504665.1:p.Ala443=
ENST00000678830.1:c.1402G=	ENSP00000504263.1:p.Ala468=
ENST00000679029.1:c.*126G=	ENSP00000504193.1:n.*126G=
ENST00000679267.1:n.3519G=
ENST00000276079.12:c.1312G=	ENSP00000276079.8:p.Ala438=
ENST00000373841.5:c.1312G=	ENSP00000362947.1:p.Ala438=
ENST00000373856.7:c.1312G=	ENSP00000362963.3:p.Ala438=
ENST00000472185.1:n.61-547G=
ENST00000473525.1:n.1086G=
ENST00000474431.5:n.347G=
ENST00000490044.5:n.2019G=
ENST00000535149.5:c.1045G=	ENSP00000441364.1:p.Ala349=
NM_001145408.1:c.1312G=	NP_001138880.1:p.Ala438=
NM_001145409.1:c.1312G=	NP_001138881.1:p.Ala438=
NM_001145410.1:c.1045G=	NP_001138882.1:p.Ala349=
NM_007363.4:c.1312G=	NP_031389.3:p.Ala438=
NM_007363.5:c.1312G= MANE Select	NP_031389.3:p.Ala438=
NM_001145408.2:c.1312G=	NP_001138880.1:p.Ala438=
NM_001145409.2:c.1312G=	NP_001138881.1:p.Ala438=
NM_001145410.2:c.1045G=	NP_001138882.1:p.Ala349=