Canonical Allele Identifier: CA331037291

Gene: NONO

Linked Data

• dbSNP Id: rs1028246479
• gnomAD v2: X-70520121-A-G
• gnomAD v3: X-71300271-A-G
• gnomAD v4: X-71300271-A-G
• MyVariant Identifiers: chrX:g.70520121A>G (hg19) ; chrX:g.71300271A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300271A>G , CM000685.2:g.71300271A>G	GRCh38
NC_000023.10:g.70520121A>G , CM000685.1:g.70520121A>G	GRCh37
NC_000023.9:g.70436846A>G	NCBI36
NG_046742.1:g.22080A>G
NG_054891.1:g.3997A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*195A>G MANE Select	ENSP00000276079.8:n.*195A>G
ENST00000420903.6:c.*195A>G	ENSP00000410299.2:n.*195A>G
ENST00000473525.2:n.2319A>G
ENST00000676495.1:n.3022A>G
ENST00000676499.1:n.2567A>G
ENST00000676797.1:c.*195A>G	ENSP00000503920.1:n.*195A>G
ENST00000677014.1:c.*1438A>G	ENSP00000503813.1:n.*1438A>G
ENST00000677218.1:n.2782A>G
ENST00000677245.1:c.*1820A>G	ENSP00000503929.1:n.*1820A>G
ENST00000677274.1:c.*195A>G	ENSP00000504314.1:n.*195A>G
ENST00000677446.1:c.*195A>G	ENSP00000503031.1:n.*195A>G
ENST00000677612.1:c.*195A>G	ENSP00000504351.1:n.*195A>G
ENST00000677766.1:n.4016A>G
ENST00000677826.1:n.2353A>G
ENST00000677879.1:c.*195A>G	ENSP00000504090.1:n.*195A>G
ENST00000677977.1:n.3443A>G
ENST00000678231.1:c.*195A>G	ENSP00000503233.1:n.*195A>G
ENST00000678323.1:n.2709A>G
ENST00000678335.1:c.*524A>G	ENSP00000503769.1:n.*524A>G
ENST00000678437.1:c.*195A>G	ENSP00000504007.1:n.*195A>G
ENST00000678660.1:c.*195A>G	ENSP00000504665.1:n.*195A>G
ENST00000678830.1:c.*195A>G	ENSP00000504263.1:n.*195A>G
ENST00000679029.1:c.*425A>G	ENSP00000504193.1:n.*425A>G
ENST00000679267.1:n.3818A>G
ENST00000276079.12:c.*195A>G	ENSP00000276079.8:n.*195A>G
ENST00000373841.5:c.*195A>G	ENSP00000362947.1:n.*195A>G
ENST00000472185.1:n.61-248A>G
ENST00000473525.1:n.1385A>G
ENST00000490044.5:n.2318A>G
ENST00000535149.5:c.*195A>G	ENSP00000441364.1:n.*195A>G
NM_001145408.1:c.*195A>G	NP_001138880.1:n.*195A>G
NM_001145409.1:c.*195A>G	NP_001138881.1:n.*195A>G
NM_001145410.1:c.*195A>G	NP_001138882.1:n.*195A>G
NM_007363.4:c.*195A>G	NP_031389.3:n.*195A>G
NM_007363.5:c.*195A>G MANE Select	NP_031389.3:n.*195A>G
NM_001145408.2:c.*195A>G	NP_001138880.1:n.*195A>G
NM_001145409.2:c.*195A>G	NP_001138881.1:n.*195A>G
NM_001145410.2:c.*195A>G	NP_001138882.1:n.*195A>G