Canonical Allele Identifier: CA413550699

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519912C>G (hg19) ; chrX:g.71300062C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300062C>G , CM000685.2:g.71300062C>G	GRCh38
NC_000023.10:g.70519912C>G , CM000685.1:g.70519912C>G	GRCh37
NC_000023.9:g.70436637C>G	NCBI36
NG_046742.1:g.21871C>G
NG_054891.1:g.3788C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1402C>G MANE Select	ENSP00000276079.8:p.Arg468Gly
ENST00000373856.8:c.1500C>G	ENSP00000362963.4:p.Asn500Lys
ENST00000420903.6:c.1402C>G	ENSP00000410299.2:p.Arg468Gly
ENST00000450092.6:c.1402C>G	ENSP00000415777.2:p.Arg468Gly
ENST00000454976.2:c.1402C>G	ENSP00000406673.2:p.Arg468Gly
ENST00000473525.2:n.2110C>G
ENST00000676495.1:n.2813C>G
ENST00000676499.1:n.2358C>G
ENST00000676797.1:c.1135C>G	ENSP00000503920.1:p.Arg379Gly
ENST00000677014.1:c.*1229C>G	ENSP00000503813.1:n.*1229C>G
ENST00000677218.1:n.2573C>G
ENST00000677245.1:c.*1611C>G	ENSP00000503929.1:n.*1611C>G
ENST00000677274.1:c.1402C>G	ENSP00000504314.1:p.Arg468Gly
ENST00000677446.1:c.1402C>G	ENSP00000503031.1:p.Arg468Gly
ENST00000677612.1:c.1402C>G	ENSP00000504351.1:p.Arg468Gly
ENST00000677766.1:n.3807C>G
ENST00000677826.1:n.2144C>G
ENST00000677879.1:c.1222C>G	ENSP00000504090.1:p.Arg408Gly
ENST00000677977.1:n.3234C>G
ENST00000678231.1:c.1402C>G	ENSP00000503233.1:p.Arg468Gly
ENST00000678323.1:n.2500C>G
ENST00000678335.1:c.*315C>G	ENSP00000503769.1:n.*315C>G
ENST00000678437.1:c.1393C>G	ENSP00000504007.1:p.Arg465Gly
ENST00000678660.1:c.1417C>G	ENSP00000504665.1:p.Arg473Gly
ENST00000678830.1:c.1492C>G	ENSP00000504263.1:p.Arg498Gly
ENST00000679029.1:c.*216C>G	ENSP00000504193.1:n.*216C>G
ENST00000679267.1:n.3609C>G
ENST00000276079.12:c.1402C>G	ENSP00000276079.8:p.Arg468Gly
ENST00000373841.5:c.1402C>G	ENSP00000362947.1:p.Arg468Gly
ENST00000373856.7:c.1402C>G	ENSP00000362963.3:p.Arg468Gly
ENST00000472185.1:n.61-457C>G
ENST00000473525.1:n.1176C>G
ENST00000474431.5:n.437C>G
ENST00000490044.5:n.2109C>G
ENST00000535149.5:c.1135C>G	ENSP00000441364.1:p.Arg379Gly
NM_001145408.1:c.1402C>G	NP_001138880.1:p.Arg468Gly
NM_001145409.1:c.1402C>G	NP_001138881.1:p.Arg468Gly
NM_001145410.1:c.1135C>G	NP_001138882.1:p.Arg379Gly
NM_007363.4:c.1402C>G	NP_031389.3:p.Arg468Gly
NM_007363.5:c.1402C>G MANE Select	NP_031389.3:p.Arg468Gly
NM_001145408.2:c.1402C>G	NP_001138880.1:p.Arg468Gly
NM_001145409.2:c.1402C>G	NP_001138881.1:p.Arg468Gly
NM_001145410.2:c.1135C>G	NP_001138882.1:p.Arg379Gly