Canonical Allele Identifier: CA413550741

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519922A>C (hg19) ; chrX:g.71300072A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300072A>C , CM000685.2:g.71300072A>C	GRCh38
NC_000023.10:g.70519922A>C , CM000685.1:g.70519922A>C	GRCh37
NC_000023.9:g.70436647A>C	NCBI36
NG_046742.1:g.21881A>C
NG_054891.1:g.3798A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1412A>C MANE Select	ENSP00000276079.8:p.Tyr471Ser
ENST00000373856.8:c.1510A>C	ENSP00000362963.4:p.Thr504Pro
ENST00000420903.6:c.1412A>C	ENSP00000410299.2:p.Tyr471Ser
ENST00000450092.6:c.1412A>C	ENSP00000415777.2:p.Tyr471Ser
ENST00000454976.2:c.1412A>C	ENSP00000406673.2:p.Tyr471Ser
ENST00000473525.2:n.2120A>C
ENST00000676495.1:n.2823A>C
ENST00000676499.1:n.2368A>C
ENST00000676797.1:c.1145A>C	ENSP00000503920.1:p.Tyr382Ser
ENST00000677014.1:c.*1239A>C	ENSP00000503813.1:n.*1239A>C
ENST00000677218.1:n.2583A>C
ENST00000677245.1:c.*1621A>C	ENSP00000503929.1:n.*1621A>C
ENST00000677274.1:c.1412A>C	ENSP00000504314.1:p.Tyr471Ser
ENST00000677446.1:c.1412A>C	ENSP00000503031.1:p.Tyr471Ser
ENST00000677612.1:c.1412A>C	ENSP00000504351.1:p.Tyr471Ser
ENST00000677766.1:n.3817A>C
ENST00000677826.1:n.2154A>C
ENST00000677879.1:c.1232A>C	ENSP00000504090.1:p.Tyr411Ser
ENST00000677977.1:n.3244A>C
ENST00000678231.1:c.1412A>C	ENSP00000503233.1:p.Tyr471Ser
ENST00000678323.1:n.2510A>C
ENST00000678335.1:c.*325A>C	ENSP00000503769.1:n.*325A>C
ENST00000678437.1:c.1403A>C	ENSP00000504007.1:p.Tyr468Ser
ENST00000678660.1:c.1427A>C	ENSP00000504665.1:p.Tyr476Ser
ENST00000678830.1:c.1502A>C	ENSP00000504263.1:p.Tyr501Ser
ENST00000679029.1:c.*226A>C	ENSP00000504193.1:n.*226A>C
ENST00000679267.1:n.3619A>C
ENST00000276079.12:c.1412A>C	ENSP00000276079.8:p.Tyr471Ser
ENST00000373841.5:c.1412A>C	ENSP00000362947.1:p.Tyr471Ser
ENST00000373856.7:c.1412A>C	ENSP00000362963.3:p.Tyr471Ser
ENST00000472185.1:n.61-447A>C
ENST00000473525.1:n.1186A>C
ENST00000474431.5:n.447A>C
ENST00000490044.5:n.2119A>C
ENST00000535149.5:c.1145A>C	ENSP00000441364.1:p.Tyr382Ser
NM_001145408.1:c.1412A>C	NP_001138880.1:p.Tyr471Ser
NM_001145409.1:c.1412A>C	NP_001138881.1:p.Tyr471Ser
NM_001145410.1:c.1145A>C	NP_001138882.1:p.Tyr382Ser
NM_007363.4:c.1412A>C	NP_031389.3:p.Tyr471Ser
NM_007363.5:c.1412A>C MANE Select	NP_031389.3:p.Tyr471Ser
NM_001145408.2:c.1412A>C	NP_001138880.1:p.Tyr471Ser
NM_001145409.2:c.1412A>C	NP_001138881.1:p.Tyr471Ser
NM_001145410.2:c.1145A>C	NP_001138882.1:p.Tyr382Ser