Canonical Allele Identifier: CA413550628

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519906A>C (hg19) ; chrX:g.71300056A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300056A>C , CM000685.2:g.71300056A>C	GRCh38
NC_000023.10:g.70519906A>C , CM000685.1:g.70519906A>C	GRCh37
NC_000023.9:g.70436631A>C	NCBI36
NG_046742.1:g.21865A>C
NG_054891.1:g.3782A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1396A>C MANE Select	ENSP00000276079.8:p.Asn466His
ENST00000373856.8:c.1494A>C	ENSP00000362963.4:p.Gln498His
ENST00000420903.6:c.1396A>C	ENSP00000410299.2:p.Asn466His
ENST00000450092.6:c.1396A>C	ENSP00000415777.2:p.Asn466His
ENST00000454976.2:c.1396A>C	ENSP00000406673.2:p.Asn466His
ENST00000473525.2:n.2104A>C
ENST00000676495.1:n.2807A>C
ENST00000676499.1:n.2352A>C
ENST00000676797.1:c.1129A>C	ENSP00000503920.1:p.Asn377His
ENST00000677014.1:c.*1223A>C	ENSP00000503813.1:n.*1223A>C
ENST00000677218.1:n.2567A>C
ENST00000677245.1:c.*1605A>C	ENSP00000503929.1:n.*1605A>C
ENST00000677274.1:c.1396A>C	ENSP00000504314.1:p.Asn466His
ENST00000677446.1:c.1396A>C	ENSP00000503031.1:p.Asn466His
ENST00000677612.1:c.1396A>C	ENSP00000504351.1:p.Asn466His
ENST00000677766.1:n.3801A>C
ENST00000677826.1:n.2138A>C
ENST00000677879.1:c.1216A>C	ENSP00000504090.1:p.Asn406His
ENST00000677977.1:n.3228A>C
ENST00000678231.1:c.1396A>C	ENSP00000503233.1:p.Asn466His
ENST00000678323.1:n.2494A>C
ENST00000678335.1:c.*309A>C	ENSP00000503769.1:n.*309A>C
ENST00000678437.1:c.1387A>C	ENSP00000504007.1:p.Asn463His
ENST00000678660.1:c.1411A>C	ENSP00000504665.1:p.Asn471His
ENST00000678830.1:c.1486A>C	ENSP00000504263.1:p.Asn496His
ENST00000679029.1:c.*210A>C	ENSP00000504193.1:n.*210A>C
ENST00000679267.1:n.3603A>C
ENST00000276079.12:c.1396A>C	ENSP00000276079.8:p.Asn466His
ENST00000373841.5:c.1396A>C	ENSP00000362947.1:p.Asn466His
ENST00000373856.7:c.1396A>C	ENSP00000362963.3:p.Asn466His
ENST00000472185.1:n.61-463A>C
ENST00000473525.1:n.1170A>C
ENST00000474431.5:n.431A>C
ENST00000490044.5:n.2103A>C
ENST00000535149.5:c.1129A>C	ENSP00000441364.1:p.Asn377His
NM_001145408.1:c.1396A>C	NP_001138880.1:p.Asn466His
NM_001145409.1:c.1396A>C	NP_001138881.1:p.Asn466His
NM_001145410.1:c.1129A>C	NP_001138882.1:p.Asn377His
NM_007363.4:c.1396A>C	NP_031389.3:p.Asn466His
NM_007363.5:c.1396A>C MANE Select	NP_031389.3:p.Asn466His
NM_001145408.2:c.1396A>C	NP_001138880.1:p.Asn466His
NM_001145409.2:c.1396A>C	NP_001138881.1:p.Asn466His
NM_001145410.2:c.1129A>C	NP_001138882.1:p.Asn377His