Canonical Allele Identifier: CA516732257

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519797A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299947A>T , CM000685.2:g.71299947A>T	GRCh38
NC_000023.10:g.70519797A>T , CM000685.1:g.70519797A>T	GRCh37
NC_000023.9:g.70436522A>T	NCBI36
NG_046742.1:g.21756A>T
NG_054891.1:g.3673A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1287A>T MANE Select	ENSP00000276079.8:p.Pro429=
ENST00000373856.8:c.1385A>T	ENSP00000362963.4:p.His462Leu
ENST00000420903.6:c.1287A>T	ENSP00000410299.2:p.Pro429=
ENST00000450092.6:c.1287A>T	ENSP00000415777.2:p.Pro429=
ENST00000454976.2:c.1287A>T	ENSP00000406673.2:p.Pro429=
ENST00000473525.2:n.1995A>T
ENST00000676495.1:n.2698A>T
ENST00000676499.1:n.2243A>T
ENST00000676797.1:c.1020A>T	ENSP00000503920.1:p.Pro340=
ENST00000677014.1:c.*1114A>T	ENSP00000503813.1:n.*1114A>T
ENST00000677218.1:n.2458A>T
ENST00000677245.1:c.*1496A>T	ENSP00000503929.1:n.*1496A>T
ENST00000677274.1:c.1287A>T	ENSP00000504314.1:p.Pro429=
ENST00000677446.1:c.1287A>T	ENSP00000503031.1:p.Pro429=
ENST00000677612.1:c.1287A>T	ENSP00000504351.1:p.Pro429=
ENST00000677766.1:n.3692A>T
ENST00000677826.1:n.2029A>T
ENST00000677879.1:c.1107A>T	ENSP00000504090.1:p.Pro369=
ENST00000677977.1:n.3119A>T
ENST00000678231.1:c.1287A>T	ENSP00000503233.1:p.Pro429=
ENST00000678323.1:n.2385A>T
ENST00000678335.1:c.*200A>T	ENSP00000503769.1:n.*200A>T
ENST00000678437.1:c.1278A>T	ENSP00000504007.1:p.Pro426=
ENST00000678660.1:c.1302A>T	ENSP00000504665.1:p.Pro434=
ENST00000678830.1:c.1377A>T	ENSP00000504263.1:p.Pro459=
ENST00000679029.1:c.*101A>T	ENSP00000504193.1:n.*101A>T
ENST00000679267.1:n.3494A>T
ENST00000276079.12:c.1287A>T	ENSP00000276079.8:p.Pro429=
ENST00000373841.5:c.1287A>T	ENSP00000362947.1:p.Pro429=
ENST00000373856.7:c.1287A>T	ENSP00000362963.3:p.Pro429=
ENST00000472185.1:n.61-572A>T
ENST00000473525.1:n.1061A>T
ENST00000474431.5:n.322A>T
ENST00000490044.5:n.1994A>T
ENST00000535149.5:c.1020A>T	ENSP00000441364.1:p.Pro340=
NM_001145408.1:c.1287A>T	NP_001138880.1:p.Pro429=
NM_001145409.1:c.1287A>T	NP_001138881.1:p.Pro429=
NM_001145410.1:c.1020A>T	NP_001138882.1:p.Pro340=
NM_007363.4:c.1287A>T	NP_031389.3:p.Pro429=
NM_007363.5:c.1287A>T MANE Select	NP_031389.3:p.Pro429=
NM_001145408.2:c.1287A>T	NP_001138880.1:p.Pro429=
NM_001145409.2:c.1287A>T	NP_001138881.1:p.Pro429=
NM_001145410.2:c.1020A>T	NP_001138882.1:p.Pro340=