Canonical Allele Identifier: CA331037203

Gene: NONO

Linked Data

• dbSNP Id: rs780790265
• gnomAD v4: X-71300139-A-AT
• MyVariant Identifiers: chrX:g.70519989_70519990insT (hg19) ; chrX:g.71300139_71300140insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300141dup , CM000685.2:g.71300141dup	GRCh38
NC_000023.10:g.70519991dup , CM000685.1:g.70519991dup	GRCh37
NC_000023.9:g.70436716dup	NCBI36
NG_046742.1:g.21950dup
NG_054891.1:g.3867dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*65dup MANE Select	ENSP00000276079.8:n.*65dup
ENST00000420903.6:c.*65dup	ENSP00000410299.2:n.*65dup
ENST00000473525.2:n.2189dup
ENST00000676495.1:n.2892dup
ENST00000676499.1:n.2437dup
ENST00000676797.1:c.*65dup	ENSP00000503920.1:n.*65dup
ENST00000677014.1:c.*1308dup	ENSP00000503813.1:n.*1308dup
ENST00000677218.1:n.2652dup
ENST00000677245.1:c.*1690dup	ENSP00000503929.1:n.*1690dup
ENST00000677274.1:c.*65dup	ENSP00000504314.1:n.*65dup
ENST00000677446.1:c.*65dup	ENSP00000503031.1:n.*65dup
ENST00000677612.1:c.*65dup	ENSP00000504351.1:n.*65dup
ENST00000677766.1:n.3886dup
ENST00000677826.1:n.2223dup
ENST00000677879.1:c.*65dup	ENSP00000504090.1:n.*65dup
ENST00000677977.1:n.3313dup
ENST00000678231.1:c.*65dup	ENSP00000503233.1:n.*65dup
ENST00000678323.1:n.2579dup
ENST00000678335.1:c.*394dup	ENSP00000503769.1:n.*394dup
ENST00000678437.1:c.*65dup	ENSP00000504007.1:n.*65dup
ENST00000678660.1:c.*65dup	ENSP00000504665.1:n.*65dup
ENST00000678830.1:c.*65dup	ENSP00000504263.1:n.*65dup
ENST00000679029.1:c.*295dup	ENSP00000504193.1:n.*295dup
ENST00000679267.1:n.3688dup
ENST00000276079.12:c.*65dup	ENSP00000276079.8:n.*65dup
ENST00000373841.5:c.*65dup	ENSP00000362947.1:n.*65dup
ENST00000373856.7:c.*65dup	ENSP00000362963.3:n.*65dup
ENST00000472185.1:n.61-378dup
ENST00000473525.1:n.1255dup
ENST00000474431.5:n.516dup
ENST00000490044.5:n.2188dup
ENST00000535149.5:c.*65dup	ENSP00000441364.1:n.*65dup
NM_001145408.1:c.*65dup	NP_001138880.1:n.*65dup
NM_001145409.1:c.*65dup	NP_001138881.1:n.*65dup
NM_001145410.1:c.*65dup	NP_001138882.1:n.*65dup
NM_007363.4:c.*65dup	NP_031389.3:n.*65dup
NM_007363.5:c.*65dup MANE Select	NP_031389.3:n.*65dup
NM_001145408.2:c.*65dup	NP_001138880.1:n.*65dup
NM_001145409.2:c.*65dup	NP_001138881.1:n.*65dup
NM_001145410.2:c.*65dup	NP_001138882.1:n.*65dup