Canonical Allele Identifier: CA413550635

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519907A>C (hg19) ; chrX:g.71300057A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300057A>C , CM000685.2:g.71300057A>C	GRCh38
NC_000023.10:g.70519907A>C , CM000685.1:g.70519907A>C	GRCh37
NC_000023.9:g.70436632A>C	NCBI36
NG_046742.1:g.21866A>C
NG_054891.1:g.3783A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1397A>C MANE Select	ENSP00000276079.8:p.Asn466Thr
ENST00000373856.8:c.1495A>C	ENSP00000362963.4:p.Thr499Pro
ENST00000420903.6:c.1397A>C	ENSP00000410299.2:p.Asn466Thr
ENST00000450092.6:c.1397A>C	ENSP00000415777.2:p.Asn466Thr
ENST00000454976.2:c.1397A>C	ENSP00000406673.2:p.Asn466Thr
ENST00000473525.2:n.2105A>C
ENST00000676495.1:n.2808A>C
ENST00000676499.1:n.2353A>C
ENST00000676797.1:c.1130A>C	ENSP00000503920.1:p.Asn377Thr
ENST00000677014.1:c.*1224A>C	ENSP00000503813.1:n.*1224A>C
ENST00000677218.1:n.2568A>C
ENST00000677245.1:c.*1606A>C	ENSP00000503929.1:n.*1606A>C
ENST00000677274.1:c.1397A>C	ENSP00000504314.1:p.Asn466Thr
ENST00000677446.1:c.1397A>C	ENSP00000503031.1:p.Asn466Thr
ENST00000677612.1:c.1397A>C	ENSP00000504351.1:p.Asn466Thr
ENST00000677766.1:n.3802A>C
ENST00000677826.1:n.2139A>C
ENST00000677879.1:c.1217A>C	ENSP00000504090.1:p.Asn406Thr
ENST00000677977.1:n.3229A>C
ENST00000678231.1:c.1397A>C	ENSP00000503233.1:p.Asn466Thr
ENST00000678323.1:n.2495A>C
ENST00000678335.1:c.*310A>C	ENSP00000503769.1:n.*310A>C
ENST00000678437.1:c.1388A>C	ENSP00000504007.1:p.Asn463Thr
ENST00000678660.1:c.1412A>C	ENSP00000504665.1:p.Asn471Thr
ENST00000678830.1:c.1487A>C	ENSP00000504263.1:p.Asn496Thr
ENST00000679029.1:c.*211A>C	ENSP00000504193.1:n.*211A>C
ENST00000679267.1:n.3604A>C
ENST00000276079.12:c.1397A>C	ENSP00000276079.8:p.Asn466Thr
ENST00000373841.5:c.1397A>C	ENSP00000362947.1:p.Asn466Thr
ENST00000373856.7:c.1397A>C	ENSP00000362963.3:p.Asn466Thr
ENST00000472185.1:n.61-462A>C
ENST00000473525.1:n.1171A>C
ENST00000474431.5:n.432A>C
ENST00000490044.5:n.2104A>C
ENST00000535149.5:c.1130A>C	ENSP00000441364.1:p.Asn377Thr
NM_001145408.1:c.1397A>C	NP_001138880.1:p.Asn466Thr
NM_001145409.1:c.1397A>C	NP_001138881.1:p.Asn466Thr
NM_001145410.1:c.1130A>C	NP_001138882.1:p.Asn377Thr
NM_007363.4:c.1397A>C	NP_031389.3:p.Asn466Thr
NM_007363.5:c.1397A>C MANE Select	NP_031389.3:p.Asn466Thr
NM_001145408.2:c.1397A>C	NP_001138880.1:p.Asn466Thr
NM_001145409.2:c.1397A>C	NP_001138881.1:p.Asn466Thr
NM_001145410.2:c.1130A>C	NP_001138882.1:p.Asn377Thr