Canonical Allele Identifier: CA413550254

Gene: NONO

Linked Data

• ClinVar Variation Id: 2579951
• ClinVar RCV Id: RCV003328926
• MyVariant Identifiers: chrX:g.70519841T>C (hg19) ; chrX:g.71299991T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299991T>C , CM000685.2:g.71299991T>C	GRCh38
NC_000023.10:g.70519841T>C , CM000685.1:g.70519841T>C	GRCh37
NC_000023.9:g.70436566T>C	NCBI36
NG_046742.1:g.21800T>C
NG_054891.1:g.3717T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1331T>C MANE Select	ENSP00000276079.8:p.Ile444Thr
ENST00000373856.8:c.1429T>C	ENSP00000362963.4:p.Leu477=
ENST00000420903.6:c.1331T>C	ENSP00000410299.2:p.Ile444Thr
ENST00000450092.6:c.1331T>C	ENSP00000415777.2:p.Ile444Thr
ENST00000454976.2:c.1331T>C	ENSP00000406673.2:p.Ile444Thr
ENST00000473525.2:n.2039T>C
ENST00000676495.1:n.2742T>C
ENST00000676499.1:n.2287T>C
ENST00000676797.1:c.1064T>C	ENSP00000503920.1:p.Ile355Thr
ENST00000677014.1:c.*1158T>C	ENSP00000503813.1:n.*1158T>C
ENST00000677218.1:n.2502T>C
ENST00000677245.1:c.*1540T>C	ENSP00000503929.1:n.*1540T>C
ENST00000677274.1:c.1331T>C	ENSP00000504314.1:p.Ile444Thr
ENST00000677446.1:c.1331T>C	ENSP00000503031.1:p.Ile444Thr
ENST00000677612.1:c.1331T>C	ENSP00000504351.1:p.Ile444Thr
ENST00000677766.1:n.3736T>C
ENST00000677826.1:n.2073T>C
ENST00000677879.1:c.1151T>C	ENSP00000504090.1:p.Ile384Thr
ENST00000677977.1:n.3163T>C
ENST00000678231.1:c.1331T>C	ENSP00000503233.1:p.Ile444Thr
ENST00000678323.1:n.2429T>C
ENST00000678335.1:c.*244T>C	ENSP00000503769.1:n.*244T>C
ENST00000678437.1:c.1322T>C	ENSP00000504007.1:p.Ile441Thr
ENST00000678660.1:c.1346T>C	ENSP00000504665.1:p.Ile449Thr
ENST00000678830.1:c.1421T>C	ENSP00000504263.1:p.Ile474Thr
ENST00000679029.1:c.*145T>C	ENSP00000504193.1:n.*145T>C
ENST00000679267.1:n.3538T>C
ENST00000276079.12:c.1331T>C	ENSP00000276079.8:p.Ile444Thr
ENST00000373841.5:c.1331T>C	ENSP00000362947.1:p.Ile444Thr
ENST00000373856.7:c.1331T>C	ENSP00000362963.3:p.Ile444Thr
ENST00000472185.1:n.61-528T>C
ENST00000473525.1:n.1105T>C
ENST00000474431.5:n.366T>C
ENST00000490044.5:n.2038T>C
ENST00000535149.5:c.1064T>C	ENSP00000441364.1:p.Ile355Thr
NM_001145408.1:c.1331T>C	NP_001138880.1:p.Ile444Thr
NM_001145409.1:c.1331T>C	NP_001138881.1:p.Ile444Thr
NM_001145410.1:c.1064T>C	NP_001138882.1:p.Ile355Thr
NM_007363.4:c.1331T>C	NP_031389.3:p.Ile444Thr
NM_007363.5:c.1331T>C MANE Select	NP_031389.3:p.Ile444Thr
NM_001145408.2:c.1331T>C	NP_001138880.1:p.Ile444Thr
NM_001145409.2:c.1331T>C	NP_001138881.1:p.Ile444Thr
NM_001145410.2:c.1064T>C	NP_001138882.1:p.Ile355Thr