Canonical Allele Identifier: CA2694039245

Gene: NONO

Linked Data

• gnomAD v4: X-71300212-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300212A>T , CM000685.2:g.71300212A>T	GRCh38
NC_000023.10:g.70520062A>T , CM000685.1:g.70520062A>T	GRCh37
NC_000023.9:g.70436787A>T	NCBI36
NG_046742.1:g.22021A>T
NG_054891.1:g.3938A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*136A>T MANE Select	ENSP00000276079.8:n.*136A>T
ENST00000420903.6:c.*136A>T	ENSP00000410299.2:n.*136A>T
ENST00000473525.2:n.2260A>T
ENST00000676495.1:n.2963A>T
ENST00000676499.1:n.2508A>T
ENST00000676797.1:c.*136A>T	ENSP00000503920.1:n.*136A>T
ENST00000677014.1:c.*1379A>T	ENSP00000503813.1:n.*1379A>T
ENST00000677218.1:n.2723A>T
ENST00000677245.1:c.*1761A>T	ENSP00000503929.1:n.*1761A>T
ENST00000677274.1:c.*136A>T	ENSP00000504314.1:n.*136A>T
ENST00000677446.1:c.*136A>T	ENSP00000503031.1:n.*136A>T
ENST00000677612.1:c.*136A>T	ENSP00000504351.1:n.*136A>T
ENST00000677766.1:n.3957A>T
ENST00000677826.1:n.2294A>T
ENST00000677879.1:c.*136A>T	ENSP00000504090.1:n.*136A>T
ENST00000677977.1:n.3384A>T
ENST00000678231.1:c.*136A>T	ENSP00000503233.1:n.*136A>T
ENST00000678323.1:n.2650A>T
ENST00000678335.1:c.*465A>T	ENSP00000503769.1:n.*465A>T
ENST00000678437.1:c.*136A>T	ENSP00000504007.1:n.*136A>T
ENST00000678660.1:c.*136A>T	ENSP00000504665.1:n.*136A>T
ENST00000678830.1:c.*136A>T	ENSP00000504263.1:n.*136A>T
ENST00000679029.1:c.*366A>T	ENSP00000504193.1:n.*366A>T
ENST00000679267.1:n.3759A>T
ENST00000276079.12:c.*136A>T	ENSP00000276079.8:n.*136A>T
ENST00000373841.5:c.*136A>T	ENSP00000362947.1:n.*136A>T
ENST00000373856.7:c.*136A>T	ENSP00000362963.3:n.*136A>T
ENST00000472185.1:n.61-307A>T
ENST00000473525.1:n.1326A>T
ENST00000474431.5:n.587A>T
ENST00000490044.5:n.2259A>T
ENST00000535149.5:c.*136A>T	ENSP00000441364.1:n.*136A>T
NM_001145408.1:c.*136A>T	NP_001138880.1:n.*136A>T
NM_001145409.1:c.*136A>T	NP_001138881.1:n.*136A>T
NM_001145410.1:c.*136A>T	NP_001138882.1:n.*136A>T
NM_007363.4:c.*136A>T	NP_031389.3:n.*136A>T
NM_007363.5:c.*136A>T MANE Select	NP_031389.3:n.*136A>T
NM_001145408.2:c.*136A>T	NP_001138880.1:n.*136A>T
NM_001145409.2:c.*136A>T	NP_001138881.1:n.*136A>T
NM_001145410.2:c.*136A>T	NP_001138882.1:n.*136A>T