Canonical Allele Identifier: CA516732375

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519851T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300001T>C , CM000685.2:g.71300001T>C	GRCh38
NC_000023.10:g.70519851T>C , CM000685.1:g.70519851T>C	GRCh37
NC_000023.9:g.70436576T>C	NCBI36
NG_046742.1:g.21810T>C
NG_054891.1:g.3727T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1341T>C MANE Select	ENSP00000276079.8:p.Ile447=
ENST00000373856.8:c.1439T>C	ENSP00000362963.4:p.Leu480Ser
ENST00000420903.6:c.1341T>C	ENSP00000410299.2:p.Ile447=
ENST00000450092.6:c.1341T>C	ENSP00000415777.2:p.Ile447=
ENST00000454976.2:c.1341T>C	ENSP00000406673.2:p.Ile447=
ENST00000473525.2:n.2049T>C
ENST00000676495.1:n.2752T>C
ENST00000676499.1:n.2297T>C
ENST00000676797.1:c.1074T>C	ENSP00000503920.1:p.Ile358=
ENST00000677014.1:c.*1168T>C	ENSP00000503813.1:n.*1168T>C
ENST00000677218.1:n.2512T>C
ENST00000677245.1:c.*1550T>C	ENSP00000503929.1:n.*1550T>C
ENST00000677274.1:c.1341T>C	ENSP00000504314.1:p.Ile447=
ENST00000677446.1:c.1341T>C	ENSP00000503031.1:p.Ile447=
ENST00000677612.1:c.1341T>C	ENSP00000504351.1:p.Ile447=
ENST00000677766.1:n.3746T>C
ENST00000677826.1:n.2083T>C
ENST00000677879.1:c.1161T>C	ENSP00000504090.1:p.Ile387=
ENST00000677977.1:n.3173T>C
ENST00000678231.1:c.1341T>C	ENSP00000503233.1:p.Ile447=
ENST00000678323.1:n.2439T>C
ENST00000678335.1:c.*254T>C	ENSP00000503769.1:n.*254T>C
ENST00000678437.1:c.1332T>C	ENSP00000504007.1:p.Ile444=
ENST00000678660.1:c.1356T>C	ENSP00000504665.1:p.Ile452=
ENST00000678830.1:c.1431T>C	ENSP00000504263.1:p.Ile477=
ENST00000679029.1:c.*155T>C	ENSP00000504193.1:n.*155T>C
ENST00000679267.1:n.3548T>C
ENST00000276079.12:c.1341T>C	ENSP00000276079.8:p.Ile447=
ENST00000373841.5:c.1341T>C	ENSP00000362947.1:p.Ile447=
ENST00000373856.7:c.1341T>C	ENSP00000362963.3:p.Ile447=
ENST00000472185.1:n.61-518T>C
ENST00000473525.1:n.1115T>C
ENST00000474431.5:n.376T>C
ENST00000490044.5:n.2048T>C
ENST00000535149.5:c.1074T>C	ENSP00000441364.1:p.Ile358=
NM_001145408.1:c.1341T>C	NP_001138880.1:p.Ile447=
NM_001145409.1:c.1341T>C	NP_001138881.1:p.Ile447=
NM_001145410.1:c.1074T>C	NP_001138882.1:p.Ile358=
NM_007363.4:c.1341T>C	NP_031389.3:p.Ile447=
NM_007363.5:c.1341T>C MANE Select	NP_031389.3:p.Ile447=
NM_001145408.2:c.1341T>C	NP_001138880.1:p.Ile447=
NM_001145409.2:c.1341T>C	NP_001138881.1:p.Ile447=
NM_001145410.2:c.1074T>C	NP_001138882.1:p.Ile358=