Canonical Allele Identifier: CA10446218

Gene: NONO

Linked Data

• dbSNP Id: rs368522598
• ExAC: X:70519897 T / C
• gnomAD v2: X-70519897-T-C
• gnomAD v3: X-71300047-T-C
• gnomAD v4: X-71300047-T-C
• MyVariant Identifiers: chrX:g.70519897T>C (hg19) ; chrX:g.71300047T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300047T>C , CM000685.2:g.71300047T>C	GRCh38
NC_000023.10:g.70519897T>C , CM000685.1:g.70519897T>C	GRCh37
NC_000023.9:g.70436622T>C	NCBI36
NG_046742.1:g.21856T>C
NG_054891.1:g.3773T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1387T>C MANE Select	ENSP00000276079.8:p.Phe463Leu
ENST00000373856.8:c.1485T>C	ENSP00000362963.4:p.Asn495=
ENST00000420903.6:c.1387T>C	ENSP00000410299.2:p.Phe463Leu
ENST00000450092.6:c.1387T>C	ENSP00000415777.2:p.Phe463Leu
ENST00000454976.2:c.1387T>C	ENSP00000406673.2:p.Phe463Leu
ENST00000473525.2:n.2095T>C
ENST00000676495.1:n.2798T>C
ENST00000676499.1:n.2343T>C
ENST00000676797.1:c.1120T>C	ENSP00000503920.1:p.Phe374Leu
ENST00000677014.1:c.*1214T>C	ENSP00000503813.1:n.*1214T>C
ENST00000677218.1:n.2558T>C
ENST00000677245.1:c.*1596T>C	ENSP00000503929.1:n.*1596T>C
ENST00000677274.1:c.1387T>C	ENSP00000504314.1:p.Phe463Leu
ENST00000677446.1:c.1387T>C	ENSP00000503031.1:p.Phe463Leu
ENST00000677612.1:c.1387T>C	ENSP00000504351.1:p.Phe463Leu
ENST00000677766.1:n.3792T>C
ENST00000677826.1:n.2129T>C
ENST00000677879.1:c.1207T>C	ENSP00000504090.1:p.Phe403Leu
ENST00000677977.1:n.3219T>C
ENST00000678231.1:c.1387T>C	ENSP00000503233.1:p.Phe463Leu
ENST00000678323.1:n.2485T>C
ENST00000678335.1:c.*300T>C	ENSP00000503769.1:n.*300T>C
ENST00000678437.1:c.1378T>C	ENSP00000504007.1:p.Phe460Leu
ENST00000678660.1:c.1402T>C	ENSP00000504665.1:p.Phe468Leu
ENST00000678830.1:c.1477T>C	ENSP00000504263.1:p.Phe493Leu
ENST00000679029.1:c.*201T>C	ENSP00000504193.1:n.*201T>C
ENST00000679267.1:n.3594T>C
ENST00000276079.12:c.1387T>C	ENSP00000276079.8:p.Phe463Leu
ENST00000373841.5:c.1387T>C	ENSP00000362947.1:p.Phe463Leu
ENST00000373856.7:c.1387T>C	ENSP00000362963.3:p.Phe463Leu
ENST00000472185.1:n.61-472T>C
ENST00000473525.1:n.1161T>C
ENST00000474431.5:n.422T>C
ENST00000490044.5:n.2094T>C
ENST00000535149.5:c.1120T>C	ENSP00000441364.1:p.Phe374Leu
NM_001145408.1:c.1387T>C	NP_001138880.1:p.Phe463Leu
NM_001145409.1:c.1387T>C	NP_001138881.1:p.Phe463Leu
NM_001145410.1:c.1120T>C	NP_001138882.1:p.Phe374Leu
NM_007363.4:c.1387T>C	NP_031389.3:p.Phe463Leu
NM_007363.5:c.1387T>C MANE Select	NP_031389.3:p.Phe463Leu
NM_001145408.2:c.1387T>C	NP_001138880.1:p.Phe463Leu
NM_001145409.2:c.1387T>C	NP_001138881.1:p.Phe463Leu
NM_001145410.2:c.1120T>C	NP_001138882.1:p.Phe374Leu