Canonical Allele Identifier: CA10446219

Gene: NONO

Linked Data

• dbSNP Id: rs752522400
• ExAC: X:70519905 A / G
• gnomAD v2: X-70519905-A-G
• gnomAD v4: X-71300055-A-G
• MyVariant Identifiers: chrX:g.70519905A>G (hg19) ; chrX:g.71300055A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300055A>G , CM000685.2:g.71300055A>G	GRCh38
NC_000023.10:g.70519905A>G , CM000685.1:g.70519905A>G	GRCh37
NC_000023.9:g.70436630A>G	NCBI36
NG_046742.1:g.21864A>G
NG_054891.1:g.3781A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1395A>G MANE Select	ENSP00000276079.8:p.Pro465=
ENST00000373856.8:c.1493A>G	ENSP00000362963.4:p.Gln498Arg
ENST00000420903.6:c.1395A>G	ENSP00000410299.2:p.Pro465=
ENST00000450092.6:c.1395A>G	ENSP00000415777.2:p.Pro465=
ENST00000454976.2:c.1395A>G	ENSP00000406673.2:p.Pro465=
ENST00000473525.2:n.2103A>G
ENST00000676495.1:n.2806A>G
ENST00000676499.1:n.2351A>G
ENST00000676797.1:c.1128A>G	ENSP00000503920.1:p.Pro376=
ENST00000677014.1:c.*1222A>G	ENSP00000503813.1:n.*1222A>G
ENST00000677218.1:n.2566A>G
ENST00000677245.1:c.*1604A>G	ENSP00000503929.1:n.*1604A>G
ENST00000677274.1:c.1395A>G	ENSP00000504314.1:p.Pro465=
ENST00000677446.1:c.1395A>G	ENSP00000503031.1:p.Pro465=
ENST00000677612.1:c.1395A>G	ENSP00000504351.1:p.Pro465=
ENST00000677766.1:n.3800A>G
ENST00000677826.1:n.2137A>G
ENST00000677879.1:c.1215A>G	ENSP00000504090.1:p.Pro405=
ENST00000677977.1:n.3227A>G
ENST00000678231.1:c.1395A>G	ENSP00000503233.1:p.Pro465=
ENST00000678323.1:n.2493A>G
ENST00000678335.1:c.*308A>G	ENSP00000503769.1:n.*308A>G
ENST00000678437.1:c.1386A>G	ENSP00000504007.1:p.Pro462=
ENST00000678660.1:c.1410A>G	ENSP00000504665.1:p.Pro470=
ENST00000678830.1:c.1485A>G	ENSP00000504263.1:p.Pro495=
ENST00000679029.1:c.*209A>G	ENSP00000504193.1:n.*209A>G
ENST00000679267.1:n.3602A>G
ENST00000276079.12:c.1395A>G	ENSP00000276079.8:p.Pro465=
ENST00000373841.5:c.1395A>G	ENSP00000362947.1:p.Pro465=
ENST00000373856.7:c.1395A>G	ENSP00000362963.3:p.Pro465=
ENST00000472185.1:n.61-464A>G
ENST00000473525.1:n.1169A>G
ENST00000474431.5:n.430A>G
ENST00000490044.5:n.2102A>G
ENST00000535149.5:c.1128A>G	ENSP00000441364.1:p.Pro376=
NM_001145408.1:c.1395A>G	NP_001138880.1:p.Pro465=
NM_001145409.1:c.1395A>G	NP_001138881.1:p.Pro465=
NM_001145410.1:c.1128A>G	NP_001138882.1:p.Pro376=
NM_007363.4:c.1395A>G	NP_031389.3:p.Pro465=
NM_007363.5:c.1395A>G MANE Select	NP_031389.3:p.Pro465=
NM_001145408.2:c.1395A>G	NP_001138880.1:p.Pro465=
NM_001145409.2:c.1395A>G	NP_001138881.1:p.Pro465=
NM_001145410.2:c.1128A>G	NP_001138882.1:p.Pro376=