Canonical Allele Identifier: CA641924891

Gene: NONO

Linked Data

• dbSNP Id: rs1474752967
• gnomAD v2: X-70519766-AGT-A
• gnomAD v4: X-71299916-AGT-A
• MyVariant Identifiers: chrX:g.70519767_70519768del (hg19) ; chrX:g.71299917_71299918del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299919_71299920del , CM000685.2:g.71299919_71299920del	GRCh38
NC_000023.10:g.70519769_70519770del , CM000685.1:g.70519769_70519770del	GRCh37
NC_000023.9:g.70436494_70436495del	NCBI36
NG_046742.1:g.21728_21729del
NG_054891.1:g.3645_3646del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1282-23_1282-22del MANE Select	ENSP00000276079.8:n.1282-23_1282-22del
ENST00000373856.8:c.1380-23_1380-22del	ENSP00000362963.4:n.1380-23_1380-22del
ENST00000420903.6:c.1282-23_1282-22del	ENSP00000410299.2:n.1282-23_1282-22del
ENST00000450092.6:c.1282-23_1282-22del	ENSP00000415777.2:n.1282-23_1282-22del
ENST00000454976.2:c.1282-23_1282-22del	ENSP00000406673.2:n.1282-23_1282-22del
ENST00000473525.2:n.1990-23_1990-22del
ENST00000676495.1:n.2693-23_2693-22del
ENST00000676499.1:n.2238-23_2238-22del
ENST00000676797.1:c.1015-23_1015-22del	ENSP00000503920.1:n.1015-23_1015-22del
ENST00000677014.1:c.*1109-23_*1109-22del	ENSP00000503813.1:n.*1109-23_*1109-22del
ENST00000677218.1:n.2453-23_2453-22del
ENST00000677245.1:c.*1491-23_*1491-22del	ENSP00000503929.1:n.*1491-23_*1491-22del
ENST00000677274.1:c.1282-23_1282-22del	ENSP00000504314.1:n.1282-23_1282-22del
ENST00000677446.1:c.1282-23_1282-22del	ENSP00000503031.1:n.1282-23_1282-22del
ENST00000677612.1:c.1282-23_1282-22del	ENSP00000504351.1:n.1282-23_1282-22del
ENST00000677766.1:n.3664_3665del
ENST00000677826.1:n.2024-23_2024-22del
ENST00000677879.1:c.1102-23_1102-22del	ENSP00000504090.1:n.1102-23_1102-22del
ENST00000677977.1:n.3114-23_3114-22del
ENST00000678231.1:c.1282-23_1282-22del	ENSP00000503233.1:n.1282-23_1282-22del
ENST00000678323.1:n.2380-23_2380-22del
ENST00000678335.1:c.*195-23_*195-22del	ENSP00000503769.1:n.*195-23_*195-22del
ENST00000678437.1:c.1273-23_1273-22del	ENSP00000504007.1:n.1273-23_1273-22del
ENST00000678660.1:c.1297-23_1297-22del	ENSP00000504665.1:n.1297-23_1297-22del
ENST00000678830.1:c.1372-23_1372-22del	ENSP00000504263.1:n.1372-23_1372-22del
ENST00000679029.1:c.*96-23_*96-22del	ENSP00000504193.1:n.*96-23_*96-22del
ENST00000679267.1:n.3466_3467del
ENST00000276079.12:c.1282-23_1282-22del	ENSP00000276079.8:n.1282-23_1282-22del
ENST00000373841.5:c.1282-23_1282-22del	ENSP00000362947.1:n.1282-23_1282-22del
ENST00000373856.7:c.1282-23_1282-22del	ENSP00000362963.3:n.1282-23_1282-22del
ENST00000472185.1:n.61-600_61-599del
ENST00000473525.1:n.1056-23_1056-22del
ENST00000474431.5:n.317-23_317-22del
ENST00000490044.5:n.1989-23_1989-22del
ENST00000535149.5:c.1015-23_1015-22del	ENSP00000441364.1:n.1015-23_1015-22del
NM_001145408.1:c.1282-23_1282-22del	NP_001138880.1:n.1282-23_1282-22del
NM_001145409.1:c.1282-23_1282-22del	NP_001138881.1:n.1282-23_1282-22del
NM_001145410.1:c.1015-23_1015-22del	NP_001138882.1:n.1015-23_1015-22del
NM_007363.4:c.1282-23_1282-22del	NP_031389.3:n.1282-23_1282-22del
NM_007363.5:c.1282-23_1282-22del MANE Select	NP_031389.3:n.1282-23_1282-22del
NM_001145408.2:c.1282-23_1282-22del	NP_001138880.1:n.1282-23_1282-22del
NM_001145409.2:c.1282-23_1282-22del	NP_001138881.1:n.1282-23_1282-22del
NM_001145410.2:c.1015-23_1015-22del	NP_001138882.1:n.1015-23_1015-22del