Canonical Allele Identifier: CA516732296

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519830A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299980A>G , CM000685.2:g.71299980A>G	GRCh38
NC_000023.10:g.70519830A>G , CM000685.1:g.70519830A>G	GRCh37
NC_000023.9:g.70436555A>G	NCBI36
NG_046742.1:g.21789A>G
NG_054891.1:g.3706A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1320A>G MANE Select	ENSP00000276079.8:p.Thr440=
ENST00000373856.8:c.1418A>G	ENSP00000362963.4:p.Gln473Arg
ENST00000420903.6:c.1320A>G	ENSP00000410299.2:p.Thr440=
ENST00000450092.6:c.1320A>G	ENSP00000415777.2:p.Thr440=
ENST00000454976.2:c.1320A>G	ENSP00000406673.2:p.Thr440=
ENST00000473525.2:n.2028A>G
ENST00000676495.1:n.2731A>G
ENST00000676499.1:n.2276A>G
ENST00000676797.1:c.1053A>G	ENSP00000503920.1:p.Thr351=
ENST00000677014.1:c.*1147A>G	ENSP00000503813.1:n.*1147A>G
ENST00000677218.1:n.2491A>G
ENST00000677245.1:c.*1529A>G	ENSP00000503929.1:n.*1529A>G
ENST00000677274.1:c.1320A>G	ENSP00000504314.1:p.Thr440=
ENST00000677446.1:c.1320A>G	ENSP00000503031.1:p.Thr440=
ENST00000677612.1:c.1320A>G	ENSP00000504351.1:p.Thr440=
ENST00000677766.1:n.3725A>G
ENST00000677826.1:n.2062A>G
ENST00000677879.1:c.1140A>G	ENSP00000504090.1:p.Thr380=
ENST00000677977.1:n.3152A>G
ENST00000678231.1:c.1320A>G	ENSP00000503233.1:p.Thr440=
ENST00000678323.1:n.2418A>G
ENST00000678335.1:c.*233A>G	ENSP00000503769.1:n.*233A>G
ENST00000678437.1:c.1311A>G	ENSP00000504007.1:p.Thr437=
ENST00000678660.1:c.1335A>G	ENSP00000504665.1:p.Thr445=
ENST00000678830.1:c.1410A>G	ENSP00000504263.1:p.Thr470=
ENST00000679029.1:c.*134A>G	ENSP00000504193.1:n.*134A>G
ENST00000679267.1:n.3527A>G
ENST00000276079.12:c.1320A>G	ENSP00000276079.8:p.Thr440=
ENST00000373841.5:c.1320A>G	ENSP00000362947.1:p.Thr440=
ENST00000373856.7:c.1320A>G	ENSP00000362963.3:p.Thr440=
ENST00000472185.1:n.61-539A>G
ENST00000473525.1:n.1094A>G
ENST00000474431.5:n.355A>G
ENST00000490044.5:n.2027A>G
ENST00000535149.5:c.1053A>G	ENSP00000441364.1:p.Thr351=
NM_001145408.1:c.1320A>G	NP_001138880.1:p.Thr440=
NM_001145409.1:c.1320A>G	NP_001138881.1:p.Thr440=
NM_001145410.1:c.1053A>G	NP_001138882.1:p.Thr351=
NM_007363.4:c.1320A>G	NP_031389.3:p.Thr440=
NM_007363.5:c.1320A>G MANE Select	NP_031389.3:p.Thr440=
NM_001145408.2:c.1320A>G	NP_001138880.1:p.Thr440=
NM_001145409.2:c.1320A>G	NP_001138881.1:p.Thr440=
NM_001145410.2:c.1053A>G	NP_001138882.1:p.Thr351=