Canonical Allele Identifier: CA2694039225

Gene: NONO

Linked Data

• gnomAD v4: X-71300188-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300188C>A , CM000685.2:g.71300188C>A	GRCh38
NC_000023.10:g.70520038C>A , CM000685.1:g.70520038C>A	GRCh37
NC_000023.9:g.70436763C>A	NCBI36
NG_046742.1:g.21997C>A
NG_054891.1:g.3914C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*112C>A MANE Select	ENSP00000276079.8:n.*112C>A
ENST00000420903.6:c.*112C>A	ENSP00000410299.2:n.*112C>A
ENST00000473525.2:n.2236C>A
ENST00000676495.1:n.2939C>A
ENST00000676499.1:n.2484C>A
ENST00000676797.1:c.*112C>A	ENSP00000503920.1:n.*112C>A
ENST00000677014.1:c.*1355C>A	ENSP00000503813.1:n.*1355C>A
ENST00000677218.1:n.2699C>A
ENST00000677245.1:c.*1737C>A	ENSP00000503929.1:n.*1737C>A
ENST00000677274.1:c.*112C>A	ENSP00000504314.1:n.*112C>A
ENST00000677446.1:c.*112C>A	ENSP00000503031.1:n.*112C>A
ENST00000677612.1:c.*112C>A	ENSP00000504351.1:n.*112C>A
ENST00000677766.1:n.3933C>A
ENST00000677826.1:n.2270C>A
ENST00000677879.1:c.*112C>A	ENSP00000504090.1:n.*112C>A
ENST00000677977.1:n.3360C>A
ENST00000678231.1:c.*112C>A	ENSP00000503233.1:n.*112C>A
ENST00000678323.1:n.2626C>A
ENST00000678335.1:c.*441C>A	ENSP00000503769.1:n.*441C>A
ENST00000678437.1:c.*112C>A	ENSP00000504007.1:n.*112C>A
ENST00000678660.1:c.*112C>A	ENSP00000504665.1:n.*112C>A
ENST00000678830.1:c.*112C>A	ENSP00000504263.1:n.*112C>A
ENST00000679029.1:c.*342C>A	ENSP00000504193.1:n.*342C>A
ENST00000679267.1:n.3735C>A
ENST00000276079.12:c.*112C>A	ENSP00000276079.8:n.*112C>A
ENST00000373841.5:c.*112C>A	ENSP00000362947.1:n.*112C>A
ENST00000373856.7:c.*112C>A	ENSP00000362963.3:n.*112C>A
ENST00000472185.1:n.61-331C>A
ENST00000473525.1:n.1302C>A
ENST00000474431.5:n.563C>A
ENST00000490044.5:n.2235C>A
ENST00000535149.5:c.*112C>A	ENSP00000441364.1:n.*112C>A
NM_001145408.1:c.*112C>A	NP_001138880.1:n.*112C>A
NM_001145409.1:c.*112C>A	NP_001138881.1:n.*112C>A
NM_001145410.1:c.*112C>A	NP_001138882.1:n.*112C>A
NM_007363.4:c.*112C>A	NP_031389.3:n.*112C>A
NM_007363.5:c.*112C>A MANE Select	NP_031389.3:n.*112C>A
NM_001145408.2:c.*112C>A	NP_001138880.1:n.*112C>A
NM_001145409.2:c.*112C>A	NP_001138881.1:n.*112C>A
NM_001145410.2:c.*112C>A	NP_001138882.1:n.*112C>A