Canonical Allele Identifier: CA413550147

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519825G>C (hg19) ; chrX:g.71299975G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299975G>C , CM000685.2:g.71299975G>C	GRCh38
NC_000023.10:g.70519825G>C , CM000685.1:g.70519825G>C	GRCh37
NC_000023.9:g.70436550G>C	NCBI36
NG_046742.1:g.21784G>C
NG_054891.1:g.3701G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1315G>C MANE Select	ENSP00000276079.8:p.Ala439Pro
ENST00000373856.8:c.1413G>C	ENSP00000362963.4:p.Leu471=
ENST00000420903.6:c.1315G>C	ENSP00000410299.2:p.Ala439Pro
ENST00000450092.6:c.1315G>C	ENSP00000415777.2:p.Ala439Pro
ENST00000454976.2:c.1315G>C	ENSP00000406673.2:p.Ala439Pro
ENST00000473525.2:n.2023G>C
ENST00000676495.1:n.2726G>C
ENST00000676499.1:n.2271G>C
ENST00000676797.1:c.1048G>C	ENSP00000503920.1:p.Ala350Pro
ENST00000677014.1:c.*1142G>C	ENSP00000503813.1:n.*1142G>C
ENST00000677218.1:n.2486G>C
ENST00000677245.1:c.*1524G>C	ENSP00000503929.1:n.*1524G>C
ENST00000677274.1:c.1315G>C	ENSP00000504314.1:p.Ala439Pro
ENST00000677446.1:c.1315G>C	ENSP00000503031.1:p.Ala439Pro
ENST00000677612.1:c.1315G>C	ENSP00000504351.1:p.Ala439Pro
ENST00000677766.1:n.3720G>C
ENST00000677826.1:n.2057G>C
ENST00000677879.1:c.1135G>C	ENSP00000504090.1:p.Ala379Pro
ENST00000677977.1:n.3147G>C
ENST00000678231.1:c.1315G>C	ENSP00000503233.1:p.Ala439Pro
ENST00000678323.1:n.2413G>C
ENST00000678335.1:c.*228G>C	ENSP00000503769.1:n.*228G>C
ENST00000678437.1:c.1306G>C	ENSP00000504007.1:p.Ala436Pro
ENST00000678660.1:c.1330G>C	ENSP00000504665.1:p.Ala444Pro
ENST00000678830.1:c.1405G>C	ENSP00000504263.1:p.Ala469Pro
ENST00000679029.1:c.*129G>C	ENSP00000504193.1:n.*129G>C
ENST00000679267.1:n.3522G>C
ENST00000276079.12:c.1315G>C	ENSP00000276079.8:p.Ala439Pro
ENST00000373841.5:c.1315G>C	ENSP00000362947.1:p.Ala439Pro
ENST00000373856.7:c.1315G>C	ENSP00000362963.3:p.Ala439Pro
ENST00000472185.1:n.61-544G>C
ENST00000473525.1:n.1089G>C
ENST00000474431.5:n.350G>C
ENST00000490044.5:n.2022G>C
ENST00000535149.5:c.1048G>C	ENSP00000441364.1:p.Ala350Pro
NM_001145408.1:c.1315G>C	NP_001138880.1:p.Ala439Pro
NM_001145409.1:c.1315G>C	NP_001138881.1:p.Ala439Pro
NM_001145410.1:c.1048G>C	NP_001138882.1:p.Ala350Pro
NM_007363.4:c.1315G>C	NP_031389.3:p.Ala439Pro
NM_007363.5:c.1315G>C MANE Select	NP_031389.3:p.Ala439Pro
NM_001145408.2:c.1315G>C	NP_001138880.1:p.Ala439Pro
NM_001145409.2:c.1315G>C	NP_001138881.1:p.Ala439Pro
NM_001145410.2:c.1048G>C	NP_001138882.1:p.Ala350Pro