Canonical Allele Identifier: CA331037122

Gene: NONO

Linked Data

• ClinVar Variation Id: 450018
• ClinVar RCV Id: RCV000522264
• dbSNP Id: rs751131066
• gnomAD v2: X-70519821-G-GGCT
• gnomAD v3: X-71299971-G-GGCT
• gnomAD v4: X-71299971-G-GGCT
• MyVariant Identifiers: chrX:g.70519825_70519827dup (hg19) ; chrX:g.70519821_70519822insGCT (hg19) ; chrX:g.71299975_71299977dup (hg38) ; chrX:g.71299971_71299972insGCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299975_71299977dup , CM000685.2:g.71299975_71299977dup	GRCh38
NC_000023.10:g.70519825_70519827dup , CM000685.1:g.70519825_70519827dup	GRCh37
NC_000023.9:g.70436550_70436552dup	NCBI36
NG_046742.1:g.21784_21786dup
NG_054891.1:g.3701_3703dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1315_1317dup MANE Select	ENSP00000276079.8:p.Ala439_Thr440insAla
ENST00000373856.8:c.1413_1415dup	ENSP00000362963.4:p.Leu472_Gln473insLeu
ENST00000420903.6:c.1315_1317dup	ENSP00000410299.2:p.Ala439_Thr440insAla
ENST00000450092.6:c.1315_1317dup	ENSP00000415777.2:p.Ala439_Thr440insAla
ENST00000454976.2:c.1315_1317dup	ENSP00000406673.2:p.Ala439_Thr440insAla
ENST00000473525.2:n.2023_2025dup
ENST00000676495.1:n.2726_2728dup
ENST00000676499.1:n.2271_2273dup
ENST00000676797.1:c.1048_1050dup	ENSP00000503920.1:p.Ala350_Thr351insAla
ENST00000677014.1:c.*1142_*1144dup	ENSP00000503813.1:n.*1142_*1144dup
ENST00000677218.1:n.2486_2488dup
ENST00000677245.1:c.*1524_*1526dup	ENSP00000503929.1:n.*1524_*1526dup
ENST00000677274.1:c.1315_1317dup	ENSP00000504314.1:p.Ala439_Thr440insAla
ENST00000677446.1:c.1315_1317dup	ENSP00000503031.1:p.Ala439_Thr440insAla
ENST00000677612.1:c.1315_1317dup	ENSP00000504351.1:p.Ala439_Thr440insAla
ENST00000677766.1:n.3720_3722dup
ENST00000677826.1:n.2057_2059dup
ENST00000677879.1:c.1135_1137dup	ENSP00000504090.1:p.Ala379_Thr380insAla
ENST00000677977.1:n.3147_3149dup
ENST00000678231.1:c.1315_1317dup	ENSP00000503233.1:p.Ala439_Thr440insAla
ENST00000678323.1:n.2413_2415dup
ENST00000678335.1:c.*228_*230dup	ENSP00000503769.1:n.*228_*230dup
ENST00000678437.1:c.1306_1308dup	ENSP00000504007.1:p.Ala436_Thr437insAla
ENST00000678660.1:c.1330_1332dup	ENSP00000504665.1:p.Ala444_Thr445insAla
ENST00000678830.1:c.1405_1407dup	ENSP00000504263.1:p.Ala469_Thr470insAla
ENST00000679029.1:c.*129_*131dup	ENSP00000504193.1:n.*129_*131dup
ENST00000679267.1:n.3522_3524dup
ENST00000276079.12:c.1315_1317dup	ENSP00000276079.8:p.Ala439_Thr440insAla
ENST00000373841.5:c.1315_1317dup	ENSP00000362947.1:p.Ala439_Thr440insAla
ENST00000373856.7:c.1315_1317dup	ENSP00000362963.3:p.Ala439_Thr440insAla
ENST00000472185.1:n.61-544_61-542dup
ENST00000473525.1:n.1089_1091dup
ENST00000474431.5:n.350_352dup
ENST00000490044.5:n.2022_2024dup
ENST00000535149.5:c.1048_1050dup	ENSP00000441364.1:p.Ala350_Thr351insAla
NM_001145408.1:c.1315_1317dup	NP_001138880.1:p.Ala439_Thr440insAla
NM_001145409.1:c.1315_1317dup	NP_001138881.1:p.Ala439_Thr440insAla
NM_001145410.1:c.1048_1050dup	NP_001138882.1:p.Ala350_Thr351insAla
NM_007363.4:c.1315_1317dup	NP_031389.3:p.Ala439_Thr440insAla
NM_007363.5:c.1315_1317dup MANE Select	NP_031389.3:p.Ala439_Thr440insAla
NM_001145408.2:c.1315_1317dup	NP_001138880.1:p.Ala439_Thr440insAla
NM_001145409.2:c.1315_1317dup	NP_001138881.1:p.Ala439_Thr440insAla
NM_001145410.2:c.1048_1050dup	NP_001138882.1:p.Ala350_Thr351insAla