Canonical Allele Identifier: CA413550361

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519859C>T (hg19) ; chrX:g.71300009C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300009C>T , CM000685.2:g.71300009C>T	GRCh38
NC_000023.10:g.70519859C>T , CM000685.1:g.70519859C>T	GRCh37
NC_000023.9:g.70436584C>T	NCBI36
NG_046742.1:g.21818C>T
NG_054891.1:g.3735C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1349C>T MANE Select	ENSP00000276079.8:p.Thr450Ile
ENST00000373856.8:c.1447C>T	ENSP00000362963.4:p.Leu483Phe
ENST00000420903.6:c.1349C>T	ENSP00000410299.2:p.Thr450Ile
ENST00000450092.6:c.1349C>T	ENSP00000415777.2:p.Thr450Ile
ENST00000454976.2:c.1349C>T	ENSP00000406673.2:p.Thr450Ile
ENST00000473525.2:n.2057C>T
ENST00000676495.1:n.2760C>T
ENST00000676499.1:n.2305C>T
ENST00000676797.1:c.1082C>T	ENSP00000503920.1:p.Thr361Ile
ENST00000677014.1:c.*1176C>T	ENSP00000503813.1:n.*1176C>T
ENST00000677218.1:n.2520C>T
ENST00000677245.1:c.*1558C>T	ENSP00000503929.1:n.*1558C>T
ENST00000677274.1:c.1349C>T	ENSP00000504314.1:p.Thr450Ile
ENST00000677446.1:c.1349C>T	ENSP00000503031.1:p.Thr450Ile
ENST00000677612.1:c.1349C>T	ENSP00000504351.1:p.Thr450Ile
ENST00000677766.1:n.3754C>T
ENST00000677826.1:n.2091C>T
ENST00000677879.1:c.1169C>T	ENSP00000504090.1:p.Thr390Ile
ENST00000677977.1:n.3181C>T
ENST00000678231.1:c.1349C>T	ENSP00000503233.1:p.Thr450Ile
ENST00000678323.1:n.2447C>T
ENST00000678335.1:c.*262C>T	ENSP00000503769.1:n.*262C>T
ENST00000678437.1:c.1340C>T	ENSP00000504007.1:p.Thr447Ile
ENST00000678660.1:c.1364C>T	ENSP00000504665.1:p.Thr455Ile
ENST00000678830.1:c.1439C>T	ENSP00000504263.1:p.Thr480Ile
ENST00000679029.1:c.*163C>T	ENSP00000504193.1:n.*163C>T
ENST00000679267.1:n.3556C>T
ENST00000276079.12:c.1349C>T	ENSP00000276079.8:p.Thr450Ile
ENST00000373841.5:c.1349C>T	ENSP00000362947.1:p.Thr450Ile
ENST00000373856.7:c.1349C>T	ENSP00000362963.3:p.Thr450Ile
ENST00000472185.1:n.61-510C>T
ENST00000473525.1:n.1123C>T
ENST00000474431.5:n.384C>T
ENST00000490044.5:n.2056C>T
ENST00000535149.5:c.1082C>T	ENSP00000441364.1:p.Thr361Ile
NM_001145408.1:c.1349C>T	NP_001138880.1:p.Thr450Ile
NM_001145409.1:c.1349C>T	NP_001138881.1:p.Thr450Ile
NM_001145410.1:c.1082C>T	NP_001138882.1:p.Thr361Ile
NM_007363.4:c.1349C>T	NP_031389.3:p.Thr450Ile
NM_007363.5:c.1349C>T MANE Select	NP_031389.3:p.Thr450Ile
NM_001145408.2:c.1349C>T	NP_001138880.1:p.Thr450Ile
NM_001145409.2:c.1349C>T	NP_001138881.1:p.Thr450Ile
NM_001145410.2:c.1082C>T	NP_001138882.1:p.Thr361Ile