Canonical Allele Identifier: CA413550738

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519921T>G (hg19) ; chrX:g.71300071T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300071T>G , CM000685.2:g.71300071T>G	GRCh38
NC_000023.10:g.70519921T>G , CM000685.1:g.70519921T>G	GRCh37
NC_000023.9:g.70436646T>G	NCBI36
NG_046742.1:g.21880T>G
NG_054891.1:g.3797T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1411T>G MANE Select	ENSP00000276079.8:p.Tyr471Asp
ENST00000373856.8:c.1509T>G	ENSP00000362963.4:p.Asp503Glu
ENST00000420903.6:c.1411T>G	ENSP00000410299.2:p.Tyr471Asp
ENST00000450092.6:c.1411T>G	ENSP00000415777.2:p.Tyr471Asp
ENST00000454976.2:c.1411T>G	ENSP00000406673.2:p.Tyr471Asp
ENST00000473525.2:n.2119T>G
ENST00000676495.1:n.2822T>G
ENST00000676499.1:n.2367T>G
ENST00000676797.1:c.1144T>G	ENSP00000503920.1:p.Tyr382Asp
ENST00000677014.1:c.*1238T>G	ENSP00000503813.1:n.*1238T>G
ENST00000677218.1:n.2582T>G
ENST00000677245.1:c.*1620T>G	ENSP00000503929.1:n.*1620T>G
ENST00000677274.1:c.1411T>G	ENSP00000504314.1:p.Tyr471Asp
ENST00000677446.1:c.1411T>G	ENSP00000503031.1:p.Tyr471Asp
ENST00000677612.1:c.1411T>G	ENSP00000504351.1:p.Tyr471Asp
ENST00000677766.1:n.3816T>G
ENST00000677826.1:n.2153T>G
ENST00000677879.1:c.1231T>G	ENSP00000504090.1:p.Tyr411Asp
ENST00000677977.1:n.3243T>G
ENST00000678231.1:c.1411T>G	ENSP00000503233.1:p.Tyr471Asp
ENST00000678323.1:n.2509T>G
ENST00000678335.1:c.*324T>G	ENSP00000503769.1:n.*324T>G
ENST00000678437.1:c.1402T>G	ENSP00000504007.1:p.Tyr468Asp
ENST00000678660.1:c.1426T>G	ENSP00000504665.1:p.Tyr476Asp
ENST00000678830.1:c.1501T>G	ENSP00000504263.1:p.Tyr501Asp
ENST00000679029.1:c.*225T>G	ENSP00000504193.1:n.*225T>G
ENST00000679267.1:n.3618T>G
ENST00000276079.12:c.1411T>G	ENSP00000276079.8:p.Tyr471Asp
ENST00000373841.5:c.1411T>G	ENSP00000362947.1:p.Tyr471Asp
ENST00000373856.7:c.1411T>G	ENSP00000362963.3:p.Tyr471Asp
ENST00000472185.1:n.61-448T>G
ENST00000473525.1:n.1185T>G
ENST00000474431.5:n.446T>G
ENST00000490044.5:n.2118T>G
ENST00000535149.5:c.1144T>G	ENSP00000441364.1:p.Tyr382Asp
NM_001145408.1:c.1411T>G	NP_001138880.1:p.Tyr471Asp
NM_001145409.1:c.1411T>G	NP_001138881.1:p.Tyr471Asp
NM_001145410.1:c.1144T>G	NP_001138882.1:p.Tyr382Asp
NM_007363.4:c.1411T>G	NP_031389.3:p.Tyr471Asp
NM_007363.5:c.1411T>G MANE Select	NP_031389.3:p.Tyr471Asp
NM_001145408.2:c.1411T>G	NP_001138880.1:p.Tyr471Asp
NM_001145409.2:c.1411T>G	NP_001138881.1:p.Tyr471Asp
NM_001145410.2:c.1144T>G	NP_001138882.1:p.Tyr382Asp