Canonical Allele Identifier: CA516728199

Gene: NONO

Linked Data

• gnomAD v4: X-71290751-A-G
• MyVariant Identifiers: chrX:g.70510601A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71290751A>G , CM000685.2:g.71290751A>G	GRCh38
NC_000023.10:g.70510601A>G , CM000685.1:g.70510601A>G	GRCh37
NC_000023.9:g.70427326A>G	NCBI36
NG_046742.1:g.12560A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000276079.13:c.114A>G MANE Select	ENSP00000276079.8:p.Pro38=
ENST00000373856.8:c.114A>G	ENSP00000362963.4:p.Pro38=
ENST00000420903.6:c.114A>G	ENSP00000410299.2:p.Pro38=
ENST00000450092.6:c.114A>G	ENSP00000415777.2:p.Pro38=
ENST00000454976.2:c.114A>G	ENSP00000406673.2:p.Pro38=
ENST00000471419.7:n.239A>G
ENST00000473525.2:n.292A>G
ENST00000676495.1:n.292A>G
ENST00000676499.1:n.292A>G
ENST00000676797.1:c.-154A>G	ENSP00000503920.1:n.-154A>G
ENST00000677014.1:c.114A>G	ENSP00000503813.1:p.Pro38=
ENST00000677218.1:n.381A>G
ENST00000677245.1:c.114A>G	ENSP00000503929.1:p.Pro38=
ENST00000677274.1:c.114A>G	ENSP00000504314.1:p.Pro38=
ENST00000677446.1:c.114A>G	ENSP00000503031.1:p.Pro38=
ENST00000677612.1:c.114A>G	ENSP00000504351.1:p.Pro38=
ENST00000677766.1:n.292A>G
ENST00000677826.1:n.292A>G
ENST00000677879.1:c.114A>G	ENSP00000504090.1:p.Pro38=
ENST00000677977.1:n.239A>G
ENST00000678231.1:c.114A>G	ENSP00000503233.1:p.Pro38=
ENST00000678323.1:n.292A>G
ENST00000678335.1:c.114A>G	ENSP00000503769.1:p.Pro38=
ENST00000678437.1:c.114A>G	ENSP00000504007.1:p.Pro38=
ENST00000678660.1:c.114A>G	ENSP00000504665.1:p.Pro38=
ENST00000678830.1:c.114A>G	ENSP00000504263.1:p.Pro38=
ENST00000679029.1:c.114A>G	ENSP00000504193.1:p.Pro38=
ENST00000679062.1:n.201A>G
ENST00000679254.1:n.289A>G
ENST00000679267.1:n.292A>G
ENST00000276079.12:c.114A>G	ENSP00000276079.8:p.Pro38=
ENST00000373841.5:c.114A>G	ENSP00000362947.1:p.Pro38=
ENST00000373856.7:c.114A>G	ENSP00000362963.3:p.Pro38=
ENST00000413858.5:c.114A>G	ENSP00000413350.1:p.Pro38=
ENST00000420903.5:c.114A>G	ENSP00000410299.1:p.Pro38=
ENST00000450092.5:c.114A>G	ENSP00000415777.1:p.Pro38=
ENST00000454976.1:c.114A>G	ENSP00000406673.1:p.Pro38=
ENST00000472185.1:n.60+6345A>G
ENST00000474431.5:n.70+7030A>G
ENST00000486613.6:n.208A>G
ENST00000535149.5:c.-113-1028A>G	ENSP00000441364.1:n.-113-1028A>G
NM_001145408.1:c.114A>G	NP_001138880.1:p.Pro38=
NM_001145409.1:c.114A>G	NP_001138881.1:p.Pro38=
NM_001145410.1:c.-113-1028A>G	NP_001138882.1:n.-113-1028A>G
NM_007363.4:c.114A>G	NP_031389.3:p.Pro38=
NM_007363.5:c.114A>G MANE Select	NP_031389.3:p.Pro38=
NM_001145408.2:c.114A>G	NP_001138880.1:p.Pro38=
NM_001145409.2:c.114A>G	NP_001138881.1:p.Pro38=
NM_001145410.2:c.-113-1028A>G	NP_001138882.1:n.-113-1028A>G