Canonical Allele Identifier: CA413550364

Gene: NONO

Linked Data

• gnomAD v4: X-71300011-C-A
• MyVariant Identifiers: chrX:g.70519861C>A (hg19) ; chrX:g.71300011C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300011C>A , CM000685.2:g.71300011C>A	GRCh38
NC_000023.10:g.70519861C>A , CM000685.1:g.70519861C>A	GRCh37
NC_000023.9:g.70436586C>A	NCBI36
NG_046742.1:g.21820C>A
NG_054891.1:g.3737C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1351C>A MANE Select	ENSP00000276079.8:p.Pro451Thr
ENST00000373856.8:c.1449C>A	ENSP00000362963.4:p.Leu483=
ENST00000420903.6:c.1351C>A	ENSP00000410299.2:p.Pro451Thr
ENST00000450092.6:c.1351C>A	ENSP00000415777.2:p.Pro451Thr
ENST00000454976.2:c.1351C>A	ENSP00000406673.2:p.Pro451Thr
ENST00000473525.2:n.2059C>A
ENST00000676495.1:n.2762C>A
ENST00000676499.1:n.2307C>A
ENST00000676797.1:c.1084C>A	ENSP00000503920.1:p.Pro362Thr
ENST00000677014.1:c.*1178C>A	ENSP00000503813.1:n.*1178C>A
ENST00000677218.1:n.2522C>A
ENST00000677245.1:c.*1560C>A	ENSP00000503929.1:n.*1560C>A
ENST00000677274.1:c.1351C>A	ENSP00000504314.1:p.Pro451Thr
ENST00000677446.1:c.1351C>A	ENSP00000503031.1:p.Pro451Thr
ENST00000677612.1:c.1351C>A	ENSP00000504351.1:p.Pro451Thr
ENST00000677766.1:n.3756C>A
ENST00000677826.1:n.2093C>A
ENST00000677879.1:c.1171C>A	ENSP00000504090.1:p.Pro391Thr
ENST00000677977.1:n.3183C>A
ENST00000678231.1:c.1351C>A	ENSP00000503233.1:p.Pro451Thr
ENST00000678323.1:n.2449C>A
ENST00000678335.1:c.*264C>A	ENSP00000503769.1:n.*264C>A
ENST00000678437.1:c.1342C>A	ENSP00000504007.1:p.Pro448Thr
ENST00000678660.1:c.1366C>A	ENSP00000504665.1:p.Pro456Thr
ENST00000678830.1:c.1441C>A	ENSP00000504263.1:p.Pro481Thr
ENST00000679029.1:c.*165C>A	ENSP00000504193.1:n.*165C>A
ENST00000679267.1:n.3558C>A
ENST00000276079.12:c.1351C>A	ENSP00000276079.8:p.Pro451Thr
ENST00000373841.5:c.1351C>A	ENSP00000362947.1:p.Pro451Thr
ENST00000373856.7:c.1351C>A	ENSP00000362963.3:p.Pro451Thr
ENST00000472185.1:n.61-508C>A
ENST00000473525.1:n.1125C>A
ENST00000474431.5:n.386C>A
ENST00000490044.5:n.2058C>A
ENST00000535149.5:c.1084C>A	ENSP00000441364.1:p.Pro362Thr
NM_001145408.1:c.1351C>A	NP_001138880.1:p.Pro451Thr
NM_001145409.1:c.1351C>A	NP_001138881.1:p.Pro451Thr
NM_001145410.1:c.1084C>A	NP_001138882.1:p.Pro362Thr
NM_007363.4:c.1351C>A	NP_031389.3:p.Pro451Thr
NM_007363.5:c.1351C>A MANE Select	NP_031389.3:p.Pro451Thr
NM_001145408.2:c.1351C>A	NP_001138880.1:p.Pro451Thr
NM_001145409.2:c.1351C>A	NP_001138881.1:p.Pro451Thr
NM_001145410.2:c.1084C>A	NP_001138882.1:p.Pro362Thr