Canonical Allele Identifier: CA10446207

Gene: NONO

Linked Data

• ClinVar Variation Id: 1659195
• ClinVar RCV Id: RCV002174575
• dbSNP Id: rs764838305
• ExAC: X:70519772 GCT / G
• gnomAD v2: X-70519772-GCT-G
• gnomAD v3: X-71299922-GCT-G
• gnomAD v4: X-71299922-GCT-G
• MyVariant Identifiers: chrX:g.70519773_70519774del (hg19) ; chrX:g.71299924_71299925del (hg38) ; chrX:g.71299923_71299924del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299927_71299928del , CM000685.2:g.71299927_71299928del	GRCh38
NC_000023.10:g.70519777_70519778del , CM000685.1:g.70519777_70519778del	GRCh37
NC_000023.9:g.70436502_70436503del	NCBI36
NG_046742.1:g.21736_21737del
NG_054891.1:g.3653_3654del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1282-15_1282-14del MANE Select	ENSP00000276079.8:n.1282-15_1282-14del
ENST00000373856.8:c.1380-15_1380-14del	ENSP00000362963.4:n.1380-15_1380-14del
ENST00000420903.6:c.1282-15_1282-14del	ENSP00000410299.2:n.1282-15_1282-14del
ENST00000450092.6:c.1282-15_1282-14del	ENSP00000415777.2:n.1282-15_1282-14del
ENST00000454976.2:c.1282-15_1282-14del	ENSP00000406673.2:n.1282-15_1282-14del
ENST00000473525.2:n.1990-15_1990-14del
ENST00000676495.1:n.2693-15_2693-14del
ENST00000676499.1:n.2238-15_2238-14del
ENST00000676797.1:c.1015-15_1015-14del	ENSP00000503920.1:n.1015-15_1015-14del
ENST00000677014.1:c.*1109-15_*1109-14del	ENSP00000503813.1:n.*1109-15_*1109-14del
ENST00000677218.1:n.2453-15_2453-14del
ENST00000677245.1:c.*1491-15_*1491-14del	ENSP00000503929.1:n.*1491-15_*1491-14del
ENST00000677274.1:c.1282-15_1282-14del	ENSP00000504314.1:n.1282-15_1282-14del
ENST00000677446.1:c.1282-15_1282-14del	ENSP00000503031.1:n.1282-15_1282-14del
ENST00000677612.1:c.1282-15_1282-14del	ENSP00000504351.1:n.1282-15_1282-14del
ENST00000677766.1:n.3672_3673del
ENST00000677826.1:n.2024-15_2024-14del
ENST00000677879.1:c.1102-15_1102-14del	ENSP00000504090.1:n.1102-15_1102-14del
ENST00000677977.1:n.3114-15_3114-14del
ENST00000678231.1:c.1282-15_1282-14del	ENSP00000503233.1:n.1282-15_1282-14del
ENST00000678323.1:n.2380-15_2380-14del
ENST00000678335.1:c.*195-15_*195-14del	ENSP00000503769.1:n.*195-15_*195-14del
ENST00000678437.1:c.1273-15_1273-14del	ENSP00000504007.1:n.1273-15_1273-14del
ENST00000678660.1:c.1297-15_1297-14del	ENSP00000504665.1:n.1297-15_1297-14del
ENST00000678830.1:c.1372-15_1372-14del	ENSP00000504263.1:n.1372-15_1372-14del
ENST00000679029.1:c.*96-15_*96-14del	ENSP00000504193.1:n.*96-15_*96-14del
ENST00000679267.1:n.3474_3475del
ENST00000276079.12:c.1282-15_1282-14del	ENSP00000276079.8:n.1282-15_1282-14del
ENST00000373841.5:c.1282-15_1282-14del	ENSP00000362947.1:n.1282-15_1282-14del
ENST00000373856.7:c.1282-15_1282-14del	ENSP00000362963.3:n.1282-15_1282-14del
ENST00000472185.1:n.61-592_61-591del
ENST00000473525.1:n.1056-15_1056-14del
ENST00000474431.5:n.317-15_317-14del
ENST00000490044.5:n.1989-15_1989-14del
ENST00000535149.5:c.1015-15_1015-14del	ENSP00000441364.1:n.1015-15_1015-14del
NM_001145408.1:c.1282-15_1282-14del	NP_001138880.1:n.1282-15_1282-14del
NM_001145409.1:c.1282-15_1282-14del	NP_001138881.1:n.1282-15_1282-14del
NM_001145410.1:c.1015-15_1015-14del	NP_001138882.1:n.1015-15_1015-14del
NM_007363.4:c.1282-15_1282-14del	NP_031389.3:n.1282-15_1282-14del
NM_007363.5:c.1282-15_1282-14del MANE Select	NP_031389.3:n.1282-15_1282-14del
NM_001145408.2:c.1282-15_1282-14del	NP_001138880.1:n.1282-15_1282-14del
NM_001145409.2:c.1282-15_1282-14del	NP_001138881.1:n.1282-15_1282-14del
NM_001145410.2:c.1015-15_1015-14del	NP_001138882.1:n.1015-15_1015-14del