Canonical Allele Identifier: CA413550052

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519814T>A (hg19) ; chrX:g.71299964T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299964T>A , CM000685.2:g.71299964T>A	GRCh38
NC_000023.10:g.70519814T>A , CM000685.1:g.70519814T>A	GRCh37
NC_000023.9:g.70436539T>A	NCBI36
NG_046742.1:g.21773T>A
NG_054891.1:g.3690T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000276079.13:c.1304T>A MANE Select	ENSP00000276079.8:p.Phe435Tyr
ENST00000373856.8:c.1402T>A	ENSP00000362963.4:p.Leu468Met
ENST00000420903.6:c.1304T>A	ENSP00000410299.2:p.Phe435Tyr
ENST00000450092.6:c.1304T>A	ENSP00000415777.2:p.Phe435Tyr
ENST00000454976.2:c.1304T>A	ENSP00000406673.2:p.Phe435Tyr
ENST00000473525.2:n.2012T>A
ENST00000676495.1:n.2715T>A
ENST00000676499.1:n.2260T>A
ENST00000676797.1:c.1037T>A	ENSP00000503920.1:p.Phe346Tyr
ENST00000677014.1:c.*1131T>A	ENSP00000503813.1:n.*1131T>A
ENST00000677218.1:n.2475T>A
ENST00000677245.1:c.*1513T>A	ENSP00000503929.1:n.*1513T>A
ENST00000677274.1:c.1304T>A	ENSP00000504314.1:p.Phe435Tyr
ENST00000677446.1:c.1304T>A	ENSP00000503031.1:p.Phe435Tyr
ENST00000677612.1:c.1304T>A	ENSP00000504351.1:p.Phe435Tyr
ENST00000677766.1:n.3709T>A
ENST00000677826.1:n.2046T>A
ENST00000677879.1:c.1124T>A	ENSP00000504090.1:p.Phe375Tyr
ENST00000677977.1:n.3136T>A
ENST00000678231.1:c.1304T>A	ENSP00000503233.1:p.Phe435Tyr
ENST00000678323.1:n.2402T>A
ENST00000678335.1:c.*217T>A	ENSP00000503769.1:n.*217T>A
ENST00000678437.1:c.1295T>A	ENSP00000504007.1:p.Phe432Tyr
ENST00000678660.1:c.1319T>A	ENSP00000504665.1:p.Phe440Tyr
ENST00000678830.1:c.1394T>A	ENSP00000504263.1:p.Phe465Tyr
ENST00000679029.1:c.*118T>A	ENSP00000504193.1:n.*118T>A
ENST00000679267.1:n.3511T>A
ENST00000276079.12:c.1304T>A	ENSP00000276079.8:p.Phe435Tyr
ENST00000373841.5:c.1304T>A	ENSP00000362947.1:p.Phe435Tyr
ENST00000373856.7:c.1304T>A	ENSP00000362963.3:p.Phe435Tyr
ENST00000472185.1:n.61-555T>A
ENST00000473525.1:n.1078T>A
ENST00000474431.5:n.339T>A
ENST00000490044.5:n.2011T>A
ENST00000535149.5:c.1037T>A	ENSP00000441364.1:p.Phe346Tyr
NM_001145408.1:c.1304T>A	NP_001138880.1:p.Phe435Tyr
NM_001145409.1:c.1304T>A	NP_001138881.1:p.Phe435Tyr
NM_001145410.1:c.1037T>A	NP_001138882.1:p.Phe346Tyr
NM_007363.4:c.1304T>A	NP_031389.3:p.Phe435Tyr
NM_007363.5:c.1304T>A MANE Select	NP_031389.3:p.Phe435Tyr
NM_001145408.2:c.1304T>A	NP_001138880.1:p.Phe435Tyr
NM_001145409.2:c.1304T>A	NP_001138881.1:p.Phe435Tyr
NM_001145410.2:c.1037T>A	NP_001138882.1:p.Phe346Tyr