Canonical Allele Identifier: CA516732772

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519914T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300064T>C , CM000685.2:g.71300064T>C	GRCh38
NC_000023.10:g.70519914T>C , CM000685.1:g.70519914T>C	GRCh37
NC_000023.9:g.70436639T>C	NCBI36
NG_046742.1:g.21873T>C
NG_054891.1:g.3790T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1404T>C MANE Select	ENSP00000276079.8:p.Arg468=
ENST00000373856.8:c.1502T>C	ENSP00000362963.4:p.Val501Ala
ENST00000420903.6:c.1404T>C	ENSP00000410299.2:p.Arg468=
ENST00000450092.6:c.1404T>C	ENSP00000415777.2:p.Arg468=
ENST00000454976.2:c.1404T>C	ENSP00000406673.2:p.Arg468=
ENST00000473525.2:n.2112T>C
ENST00000676495.1:n.2815T>C
ENST00000676499.1:n.2360T>C
ENST00000676797.1:c.1137T>C	ENSP00000503920.1:p.Arg379=
ENST00000677014.1:c.*1231T>C	ENSP00000503813.1:n.*1231T>C
ENST00000677218.1:n.2575T>C
ENST00000677245.1:c.*1613T>C	ENSP00000503929.1:n.*1613T>C
ENST00000677274.1:c.1404T>C	ENSP00000504314.1:p.Arg468=
ENST00000677446.1:c.1404T>C	ENSP00000503031.1:p.Arg468=
ENST00000677612.1:c.1404T>C	ENSP00000504351.1:p.Arg468=
ENST00000677766.1:n.3809T>C
ENST00000677826.1:n.2146T>C
ENST00000677879.1:c.1224T>C	ENSP00000504090.1:p.Arg408=
ENST00000677977.1:n.3236T>C
ENST00000678231.1:c.1404T>C	ENSP00000503233.1:p.Arg468=
ENST00000678323.1:n.2502T>C
ENST00000678335.1:c.*317T>C	ENSP00000503769.1:n.*317T>C
ENST00000678437.1:c.1395T>C	ENSP00000504007.1:p.Arg465=
ENST00000678660.1:c.1419T>C	ENSP00000504665.1:p.Arg473=
ENST00000678830.1:c.1494T>C	ENSP00000504263.1:p.Arg498=
ENST00000679029.1:c.*218T>C	ENSP00000504193.1:n.*218T>C
ENST00000679267.1:n.3611T>C
ENST00000276079.12:c.1404T>C	ENSP00000276079.8:p.Arg468=
ENST00000373841.5:c.1404T>C	ENSP00000362947.1:p.Arg468=
ENST00000373856.7:c.1404T>C	ENSP00000362963.3:p.Arg468=
ENST00000472185.1:n.61-455T>C
ENST00000473525.1:n.1178T>C
ENST00000474431.5:n.439T>C
ENST00000490044.5:n.2111T>C
ENST00000535149.5:c.1137T>C	ENSP00000441364.1:p.Arg379=
NM_001145408.1:c.1404T>C	NP_001138880.1:p.Arg468=
NM_001145409.1:c.1404T>C	NP_001138881.1:p.Arg468=
NM_001145410.1:c.1137T>C	NP_001138882.1:p.Arg379=
NM_007363.4:c.1404T>C	NP_031389.3:p.Arg468=
NM_007363.5:c.1404T>C MANE Select	NP_031389.3:p.Arg468=
NM_001145408.2:c.1404T>C	NP_001138880.1:p.Arg468=
NM_001145409.2:c.1404T>C	NP_001138881.1:p.Arg468=
NM_001145410.2:c.1137T>C	NP_001138882.1:p.Arg379=