Canonical Allele Identifier: CA413550138

Gene: NONO

Linked Data

• dbSNP Id: rs1409992583
• gnomAD v2: X-70519823-C-T
• gnomAD v4: X-71299973-C-T
• MyVariant Identifiers: chrX:g.70519823C>T (hg19) ; chrX:g.71299973C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299973C>T , CM000685.2:g.71299973C>T	GRCh38
NC_000023.10:g.70519823C>T , CM000685.1:g.70519823C>T	GRCh37
NC_000023.9:g.70436548C>T	NCBI36
NG_046742.1:g.21782C>T
NG_054891.1:g.3699C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1313C>T MANE Select	ENSP00000276079.8:p.Ala438Val
ENST00000373856.8:c.1411C>T	ENSP00000362963.4:p.Leu471=
ENST00000420903.6:c.1313C>T	ENSP00000410299.2:p.Ala438Val
ENST00000450092.6:c.1313C>T	ENSP00000415777.2:p.Ala438Val
ENST00000454976.2:c.1313C>T	ENSP00000406673.2:p.Ala438Val
ENST00000473525.2:n.2021C>T
ENST00000676495.1:n.2724C>T
ENST00000676499.1:n.2269C>T
ENST00000676797.1:c.1046C>T	ENSP00000503920.1:p.Ala349Val
ENST00000677014.1:c.*1140C>T	ENSP00000503813.1:n.*1140C>T
ENST00000677218.1:n.2484C>T
ENST00000677245.1:c.*1522C>T	ENSP00000503929.1:n.*1522C>T
ENST00000677274.1:c.1313C>T	ENSP00000504314.1:p.Ala438Val
ENST00000677446.1:c.1313C>T	ENSP00000503031.1:p.Ala438Val
ENST00000677612.1:c.1313C>T	ENSP00000504351.1:p.Ala438Val
ENST00000677766.1:n.3718C>T
ENST00000677826.1:n.2055C>T
ENST00000677879.1:c.1133C>T	ENSP00000504090.1:p.Ala378Val
ENST00000677977.1:n.3145C>T
ENST00000678231.1:c.1313C>T	ENSP00000503233.1:p.Ala438Val
ENST00000678323.1:n.2411C>T
ENST00000678335.1:c.*226C>T	ENSP00000503769.1:n.*226C>T
ENST00000678437.1:c.1304C>T	ENSP00000504007.1:p.Ala435Val
ENST00000678660.1:c.1328C>T	ENSP00000504665.1:p.Ala443Val
ENST00000678830.1:c.1403C>T	ENSP00000504263.1:p.Ala468Val
ENST00000679029.1:c.*127C>T	ENSP00000504193.1:n.*127C>T
ENST00000679267.1:n.3520C>T
ENST00000276079.12:c.1313C>T	ENSP00000276079.8:p.Ala438Val
ENST00000373841.5:c.1313C>T	ENSP00000362947.1:p.Ala438Val
ENST00000373856.7:c.1313C>T	ENSP00000362963.3:p.Ala438Val
ENST00000472185.1:n.61-546C>T
ENST00000473525.1:n.1087C>T
ENST00000474431.5:n.348C>T
ENST00000490044.5:n.2020C>T
ENST00000535149.5:c.1046C>T	ENSP00000441364.1:p.Ala349Val
NM_001145408.1:c.1313C>T	NP_001138880.1:p.Ala438Val
NM_001145409.1:c.1313C>T	NP_001138881.1:p.Ala438Val
NM_001145410.1:c.1046C>T	NP_001138882.1:p.Ala349Val
NM_007363.4:c.1313C>T	NP_031389.3:p.Ala438Val
NM_007363.5:c.1313C>T MANE Select	NP_031389.3:p.Ala438Val
NM_001145408.2:c.1313C>T	NP_001138880.1:p.Ala438Val
NM_001145409.2:c.1313C>T	NP_001138881.1:p.Ala438Val
NM_001145410.2:c.1046C>T	NP_001138882.1:p.Ala349Val