Canonical Allele Identifier: CA877831731

Gene: NONO

Linked Data

• dbSNP Id: rs1225024327
• gnomAD v3: X-71299913-T-TAC
• gnomAD v4: X-71299913-T-TAC
• MyVariant Identifiers: chrX:g.70519763_70519764insAC (hg19) ; chrX:g.71299913_71299914insAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299915_71299916dup , CM000685.2:g.71299915_71299916dup	GRCh38
NC_000023.10:g.70519765_70519766dup , CM000685.1:g.70519765_70519766dup	GRCh37
NC_000023.9:g.70436490_70436491dup	NCBI36
NG_046742.1:g.21724_21725dup
NG_054891.1:g.3641_3642dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1282-27_1282-26dup MANE Select	ENSP00000276079.8:n.1282-27_1282-26dup
ENST00000373856.8:c.1380-27_1380-26dup	ENSP00000362963.4:n.1380-27_1380-26dup
ENST00000420903.6:c.1282-27_1282-26dup	ENSP00000410299.2:n.1282-27_1282-26dup
ENST00000450092.6:c.1282-27_1282-26dup	ENSP00000415777.2:n.1282-27_1282-26dup
ENST00000454976.2:c.1282-27_1282-26dup	ENSP00000406673.2:n.1282-27_1282-26dup
ENST00000473525.2:n.1990-27_1990-26dup
ENST00000676495.1:n.2693-27_2693-26dup
ENST00000676499.1:n.2238-27_2238-26dup
ENST00000676797.1:c.1015-27_1015-26dup	ENSP00000503920.1:n.1015-27_1015-26dup
ENST00000677014.1:c.*1109-27_*1109-26dup	ENSP00000503813.1:n.*1109-27_*1109-26dup
ENST00000677218.1:n.2453-27_2453-26dup
ENST00000677245.1:c.*1491-27_*1491-26dup	ENSP00000503929.1:n.*1491-27_*1491-26dup
ENST00000677274.1:c.1282-27_1282-26dup	ENSP00000504314.1:n.1282-27_1282-26dup
ENST00000677446.1:c.1282-27_1282-26dup	ENSP00000503031.1:n.1282-27_1282-26dup
ENST00000677612.1:c.1282-27_1282-26dup	ENSP00000504351.1:n.1282-27_1282-26dup
ENST00000677766.1:n.3660_3661dup
ENST00000677826.1:n.2024-27_2024-26dup
ENST00000677879.1:c.1102-27_1102-26dup	ENSP00000504090.1:n.1102-27_1102-26dup
ENST00000677977.1:n.3114-27_3114-26dup
ENST00000678231.1:c.1282-27_1282-26dup	ENSP00000503233.1:n.1282-27_1282-26dup
ENST00000678323.1:n.2380-27_2380-26dup
ENST00000678335.1:c.*195-27_*195-26dup	ENSP00000503769.1:n.*195-27_*195-26dup
ENST00000678437.1:c.1273-27_1273-26dup	ENSP00000504007.1:n.1273-27_1273-26dup
ENST00000678660.1:c.1297-27_1297-26dup	ENSP00000504665.1:n.1297-27_1297-26dup
ENST00000678830.1:c.1372-27_1372-26dup	ENSP00000504263.1:n.1372-27_1372-26dup
ENST00000679029.1:c.*96-27_*96-26dup	ENSP00000504193.1:n.*96-27_*96-26dup
ENST00000679267.1:n.3462_3463dup
ENST00000276079.12:c.1282-27_1282-26dup	ENSP00000276079.8:n.1282-27_1282-26dup
ENST00000373841.5:c.1282-27_1282-26dup	ENSP00000362947.1:n.1282-27_1282-26dup
ENST00000373856.7:c.1282-27_1282-26dup	ENSP00000362963.3:n.1282-27_1282-26dup
ENST00000472185.1:n.61-604_61-603dup
ENST00000473525.1:n.1056-27_1056-26dup
ENST00000474431.5:n.317-27_317-26dup
ENST00000490044.5:n.1989-27_1989-26dup
ENST00000535149.5:c.1015-27_1015-26dup	ENSP00000441364.1:n.1015-27_1015-26dup
NM_001145408.1:c.1282-27_1282-26dup	NP_001138880.1:n.1282-27_1282-26dup
NM_001145409.1:c.1282-27_1282-26dup	NP_001138881.1:n.1282-27_1282-26dup
NM_001145410.1:c.1015-27_1015-26dup	NP_001138882.1:n.1015-27_1015-26dup
NM_007363.4:c.1282-27_1282-26dup	NP_031389.3:n.1282-27_1282-26dup
NM_007363.5:c.1282-27_1282-26dup MANE Select	NP_031389.3:n.1282-27_1282-26dup
NM_001145408.2:c.1282-27_1282-26dup	NP_001138880.1:n.1282-27_1282-26dup
NM_001145409.2:c.1282-27_1282-26dup	NP_001138881.1:n.1282-27_1282-26dup
NM_001145410.2:c.1015-27_1015-26dup	NP_001138882.1:n.1015-27_1015-26dup