Canonical Allele Identifier: CA641924915

Gene: NONO

Linked Data

• dbSNP Id: rs1427200927
• gnomAD v2: X-70520107-ATTCTGTGTGGTATATTGTTTAATCAG-A
• gnomAD v3: X-71300257-ATTCTGTGTGGTATATTGTTTAATCAG-A
• gnomAD v4: X-71300257-ATTCTGTGTGGTATATTGTTTAATCAG-A
• MyVariant Identifiers: chrX:g.70520108_70520133del (hg19) ; chrX:g.71300258_71300283del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300269_71300294del , CM000685.2:g.71300269_71300294del	GRCh38
NC_000023.10:g.70520119_70520144del , CM000685.1:g.70520119_70520144del	GRCh37
NC_000023.9:g.70436844_70436869del	NCBI36
NG_046742.1:g.22078_22103del
NG_054891.1:g.3995_4020del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*193_*218del MANE Select	ENSP00000276079.8:n.*193_*218del
ENST00000420903.6:c.*193_*218del	ENSP00000410299.2:n.*193_*218del
ENST00000473525.2:n.2317_2342del
ENST00000676495.1:n.3020_3045del
ENST00000676499.1:n.2565_2590del
ENST00000676797.1:c.*193_*218del	ENSP00000503920.1:n.*193_*218del
ENST00000677014.1:c.*1436_*1461del	ENSP00000503813.1:n.*1436_*1461del
ENST00000677218.1:n.2780_2805del
ENST00000677245.1:c.*1818_*1843del	ENSP00000503929.1:n.*1818_*1843del
ENST00000677274.1:c.*193_*218del	ENSP00000504314.1:n.*193_*218del
ENST00000677446.1:c.*193_*218del	ENSP00000503031.1:n.*193_*218del
ENST00000677612.1:c.*193_*218del	ENSP00000504351.1:n.*193_*218del
ENST00000677766.1:n.4014_4039del
ENST00000677826.1:n.2351_2376del
ENST00000677879.1:c.*193_*218del	ENSP00000504090.1:n.*193_*218del
ENST00000677977.1:n.3441_3466del
ENST00000678231.1:c.*193_*218del	ENSP00000503233.1:n.*193_*218del
ENST00000678323.1:n.2707_2732del
ENST00000678335.1:c.*522_*547del	ENSP00000503769.1:n.*522_*547del
ENST00000678437.1:c.*193_*218del	ENSP00000504007.1:n.*193_*218del
ENST00000678660.1:c.*193_*218del	ENSP00000504665.1:n.*193_*218del
ENST00000678830.1:c.*193_*218del	ENSP00000504263.1:n.*193_*218del
ENST00000679029.1:c.*423_*448del	ENSP00000504193.1:n.*423_*448del
ENST00000679267.1:n.3816_3841del
ENST00000276079.12:c.*193_*218del	ENSP00000276079.8:n.*193_*218del
ENST00000373841.5:c.*193_*218del	ENSP00000362947.1:n.*193_*218del
ENST00000472185.1:n.61-250_61-225del
ENST00000473525.1:n.1383_1408del
ENST00000490044.5:n.2316_2341del
ENST00000535149.5:c.*193_*218del	ENSP00000441364.1:n.*193_*218del
NM_001145408.1:c.*193_*218del	NP_001138880.1:n.*193_*218del
NM_001145409.1:c.*193_*218del	NP_001138881.1:n.*193_*218del
NM_001145410.1:c.*193_*218del	NP_001138882.1:n.*193_*218del
NM_007363.4:c.*193_*218del	NP_031389.3:n.*193_*218del
NM_007363.5:c.*193_*218del MANE Select	NP_031389.3:n.*193_*218del
NM_001145408.2:c.*193_*218del	NP_001138880.1:n.*193_*218del
NM_001145409.2:c.*193_*218del	NP_001138881.1:n.*193_*218del
NM_001145410.2:c.*193_*218del	NP_001138882.1:n.*193_*218del