Canonical Allele Identifier: CA516732456

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519866T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300016T>G , CM000685.2:g.71300016T>G	GRCh38
NC_000023.10:g.70519866T>G , CM000685.1:g.70519866T>G	GRCh37
NC_000023.9:g.70436591T>G	NCBI36
NG_046742.1:g.21825T>G
NG_054891.1:g.3742T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1356T>G MANE Select	ENSP00000276079.8:p.Pro452=
ENST00000373856.8:c.1454T>G	ENSP00000362963.4:p.Leu485Arg
ENST00000420903.6:c.1356T>G	ENSP00000410299.2:p.Pro452=
ENST00000450092.6:c.1356T>G	ENSP00000415777.2:p.Pro452=
ENST00000454976.2:c.1356T>G	ENSP00000406673.2:p.Pro452=
ENST00000473525.2:n.2064T>G
ENST00000676495.1:n.2767T>G
ENST00000676499.1:n.2312T>G
ENST00000676797.1:c.1089T>G	ENSP00000503920.1:p.Pro363=
ENST00000677014.1:c.*1183T>G	ENSP00000503813.1:n.*1183T>G
ENST00000677218.1:n.2527T>G
ENST00000677245.1:c.*1565T>G	ENSP00000503929.1:n.*1565T>G
ENST00000677274.1:c.1356T>G	ENSP00000504314.1:p.Pro452=
ENST00000677446.1:c.1356T>G	ENSP00000503031.1:p.Pro452=
ENST00000677612.1:c.1356T>G	ENSP00000504351.1:p.Pro452=
ENST00000677766.1:n.3761T>G
ENST00000677826.1:n.2098T>G
ENST00000677879.1:c.1176T>G	ENSP00000504090.1:p.Pro392=
ENST00000677977.1:n.3188T>G
ENST00000678231.1:c.1356T>G	ENSP00000503233.1:p.Pro452=
ENST00000678323.1:n.2454T>G
ENST00000678335.1:c.*269T>G	ENSP00000503769.1:n.*269T>G
ENST00000678437.1:c.1347T>G	ENSP00000504007.1:p.Pro449=
ENST00000678660.1:c.1371T>G	ENSP00000504665.1:p.Pro457=
ENST00000678830.1:c.1446T>G	ENSP00000504263.1:p.Pro482=
ENST00000679029.1:c.*170T>G	ENSP00000504193.1:n.*170T>G
ENST00000679267.1:n.3563T>G
ENST00000276079.12:c.1356T>G	ENSP00000276079.8:p.Pro452=
ENST00000373841.5:c.1356T>G	ENSP00000362947.1:p.Pro452=
ENST00000373856.7:c.1356T>G	ENSP00000362963.3:p.Pro452=
ENST00000472185.1:n.61-503T>G
ENST00000473525.1:n.1130T>G
ENST00000474431.5:n.391T>G
ENST00000490044.5:n.2063T>G
ENST00000535149.5:c.1089T>G	ENSP00000441364.1:p.Pro363=
NM_001145408.1:c.1356T>G	NP_001138880.1:p.Pro452=
NM_001145409.1:c.1356T>G	NP_001138881.1:p.Pro452=
NM_001145410.1:c.1089T>G	NP_001138882.1:p.Pro363=
NM_007363.4:c.1356T>G	NP_031389.3:p.Pro452=
NM_007363.5:c.1356T>G MANE Select	NP_031389.3:p.Pro452=
NM_001145408.2:c.1356T>G	NP_001138880.1:p.Pro452=
NM_001145409.2:c.1356T>G	NP_001138881.1:p.Pro452=
NM_001145410.2:c.1089T>G	NP_001138882.1:p.Pro363=