Canonical Allele Identifier: CA877832022

Gene: NONO

Linked Data

• dbSNP Id: rs1332386571
• gnomAD v3: X-71300246-TAAAC-T
• gnomAD v4: X-71300246-TAAAC-T
• MyVariant Identifiers: chrX:g.70520097_70520100del (hg19) ; chrX:g.71300247_71300250del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300249_71300252del , CM000685.2:g.71300249_71300252del	GRCh38
NC_000023.10:g.70520099_70520102del , CM000685.1:g.70520099_70520102del	GRCh37
NC_000023.9:g.70436824_70436827del	NCBI36
NG_046742.1:g.22058_22061del
NG_054891.1:g.3975_3978del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*173_*176del MANE Select	ENSP00000276079.8:n.*173_*176del
ENST00000420903.6:c.*173_*176del	ENSP00000410299.2:n.*173_*176del
ENST00000473525.2:n.2297_2300del
ENST00000676495.1:n.3000_3003del
ENST00000676499.1:n.2545_2548del
ENST00000676797.1:c.*173_*176del	ENSP00000503920.1:n.*173_*176del
ENST00000677014.1:c.*1416_*1419del	ENSP00000503813.1:n.*1416_*1419del
ENST00000677218.1:n.2760_2763del
ENST00000677245.1:c.*1798_*1801del	ENSP00000503929.1:n.*1798_*1801del
ENST00000677274.1:c.*173_*176del	ENSP00000504314.1:n.*173_*176del
ENST00000677446.1:c.*173_*176del	ENSP00000503031.1:n.*173_*176del
ENST00000677612.1:c.*173_*176del	ENSP00000504351.1:n.*173_*176del
ENST00000677766.1:n.3994_3997del
ENST00000677826.1:n.2331_2334del
ENST00000677879.1:c.*173_*176del	ENSP00000504090.1:n.*173_*176del
ENST00000677977.1:n.3421_3424del
ENST00000678231.1:c.*173_*176del	ENSP00000503233.1:n.*173_*176del
ENST00000678323.1:n.2687_2690del
ENST00000678335.1:c.*502_*505del	ENSP00000503769.1:n.*502_*505del
ENST00000678437.1:c.*173_*176del	ENSP00000504007.1:n.*173_*176del
ENST00000678660.1:c.*173_*176del	ENSP00000504665.1:n.*173_*176del
ENST00000678830.1:c.*173_*176del	ENSP00000504263.1:n.*173_*176del
ENST00000679029.1:c.*403_*406del	ENSP00000504193.1:n.*403_*406del
ENST00000679267.1:n.3796_3799del
ENST00000276079.12:c.*173_*176del	ENSP00000276079.8:n.*173_*176del
ENST00000373841.5:c.*173_*176del	ENSP00000362947.1:n.*173_*176del
ENST00000373856.7:c.*173_*176del	ENSP00000362963.3:n.*173_*176del
ENST00000472185.1:n.61-270_61-267del
ENST00000473525.1:n.1363_1366del
ENST00000474431.5:n.624_627del
ENST00000490044.5:n.2296_2299del
ENST00000535149.5:c.*173_*176del	ENSP00000441364.1:n.*173_*176del
NM_001145408.1:c.*173_*176del	NP_001138880.1:n.*173_*176del
NM_001145409.1:c.*173_*176del	NP_001138881.1:n.*173_*176del
NM_001145410.1:c.*173_*176del	NP_001138882.1:n.*173_*176del
NM_007363.4:c.*173_*176del	NP_031389.3:n.*173_*176del
NM_007363.5:c.*173_*176del MANE Select	NP_031389.3:n.*173_*176del
NM_001145408.2:c.*173_*176del	NP_001138880.1:n.*173_*176del
NM_001145409.2:c.*173_*176del	NP_001138881.1:n.*173_*176del
NM_001145410.2:c.*173_*176del	NP_001138882.1:n.*173_*176del