Canonical Allele Identifier: CA413549976

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519802C>G (hg19) ; chrX:g.71299952C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299952C>G , CM000685.2:g.71299952C>G	GRCh38
NC_000023.10:g.70519802C>G , CM000685.1:g.70519802C>G	GRCh37
NC_000023.9:g.70436527C>G	NCBI36
NG_046742.1:g.21761C>G
NG_054891.1:g.3678C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000276079.13:c.1292C>G MANE Select	ENSP00000276079.8:p.Thr431Arg
ENST00000373856.8:c.1390C>G	ENSP00000362963.4:p.Gln464Glu
ENST00000420903.6:c.1292C>G	ENSP00000410299.2:p.Thr431Arg
ENST00000450092.6:c.1292C>G	ENSP00000415777.2:p.Thr431Arg
ENST00000454976.2:c.1292C>G	ENSP00000406673.2:p.Thr431Arg
ENST00000473525.2:n.2000C>G
ENST00000676495.1:n.2703C>G
ENST00000676499.1:n.2248C>G
ENST00000676797.1:c.1025C>G	ENSP00000503920.1:p.Thr342Arg
ENST00000677014.1:c.*1119C>G	ENSP00000503813.1:n.*1119C>G
ENST00000677218.1:n.2463C>G
ENST00000677245.1:c.*1501C>G	ENSP00000503929.1:n.*1501C>G
ENST00000677274.1:c.1292C>G	ENSP00000504314.1:p.Thr431Arg
ENST00000677446.1:c.1292C>G	ENSP00000503031.1:p.Thr431Arg
ENST00000677612.1:c.1292C>G	ENSP00000504351.1:p.Thr431Arg
ENST00000677766.1:n.3697C>G
ENST00000677826.1:n.2034C>G
ENST00000677879.1:c.1112C>G	ENSP00000504090.1:p.Thr371Arg
ENST00000677977.1:n.3124C>G
ENST00000678231.1:c.1292C>G	ENSP00000503233.1:p.Thr431Arg
ENST00000678323.1:n.2390C>G
ENST00000678335.1:c.*205C>G	ENSP00000503769.1:n.*205C>G
ENST00000678437.1:c.1283C>G	ENSP00000504007.1:p.Thr428Arg
ENST00000678660.1:c.1307C>G	ENSP00000504665.1:p.Thr436Arg
ENST00000678830.1:c.1382C>G	ENSP00000504263.1:p.Thr461Arg
ENST00000679029.1:c.*106C>G	ENSP00000504193.1:n.*106C>G
ENST00000679267.1:n.3499C>G
ENST00000276079.12:c.1292C>G	ENSP00000276079.8:p.Thr431Arg
ENST00000373841.5:c.1292C>G	ENSP00000362947.1:p.Thr431Arg
ENST00000373856.7:c.1292C>G	ENSP00000362963.3:p.Thr431Arg
ENST00000472185.1:n.61-567C>G
ENST00000473525.1:n.1066C>G
ENST00000474431.5:n.327C>G
ENST00000490044.5:n.1999C>G
ENST00000535149.5:c.1025C>G	ENSP00000441364.1:p.Thr342Arg
NM_001145408.1:c.1292C>G	NP_001138880.1:p.Thr431Arg
NM_001145409.1:c.1292C>G	NP_001138881.1:p.Thr431Arg
NM_001145410.1:c.1025C>G	NP_001138882.1:p.Thr342Arg
NM_007363.4:c.1292C>G	NP_031389.3:p.Thr431Arg
NM_007363.5:c.1292C>G MANE Select	NP_031389.3:p.Thr431Arg
NM_001145408.2:c.1292C>G	NP_001138880.1:p.Thr431Arg
NM_001145409.2:c.1292C>G	NP_001138881.1:p.Thr431Arg
NM_001145410.2:c.1025C>G	NP_001138882.1:p.Thr342Arg