Canonical Allele Identifier: CA331037270

Gene: NONO

Linked Data

• dbSNP Id: rs1000131078
• MyVariant Identifiers: chrX:g.71300228G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300228G>A , CM000685.2:g.71300228G>A	GRCh38
NC_000023.10:g.70520078G>A , CM000685.1:g.70520078G>A	GRCh37
NC_000023.9:g.70436803G>A	NCBI36
NG_046742.1:g.22037G>A
NG_054891.1:g.3954G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*152G>A MANE Select	ENSP00000276079.8:n.*152G>A
ENST00000420903.6:c.*152G>A	ENSP00000410299.2:n.*152G>A
ENST00000473525.2:n.2276G>A
ENST00000676495.1:n.2979G>A
ENST00000676499.1:n.2524G>A
ENST00000676797.1:c.*152G>A	ENSP00000503920.1:n.*152G>A
ENST00000677014.1:c.*1395G>A	ENSP00000503813.1:n.*1395G>A
ENST00000677218.1:n.2739G>A
ENST00000677245.1:c.*1777G>A	ENSP00000503929.1:n.*1777G>A
ENST00000677274.1:c.*152G>A	ENSP00000504314.1:n.*152G>A
ENST00000677446.1:c.*152G>A	ENSP00000503031.1:n.*152G>A
ENST00000677612.1:c.*152G>A	ENSP00000504351.1:n.*152G>A
ENST00000677766.1:n.3973G>A
ENST00000677826.1:n.2310G>A
ENST00000677879.1:c.*152G>A	ENSP00000504090.1:n.*152G>A
ENST00000677977.1:n.3400G>A
ENST00000678231.1:c.*152G>A	ENSP00000503233.1:n.*152G>A
ENST00000678323.1:n.2666G>A
ENST00000678335.1:c.*481G>A	ENSP00000503769.1:n.*481G>A
ENST00000678437.1:c.*152G>A	ENSP00000504007.1:n.*152G>A
ENST00000678660.1:c.*152G>A	ENSP00000504665.1:n.*152G>A
ENST00000678830.1:c.*152G>A	ENSP00000504263.1:n.*152G>A
ENST00000679029.1:c.*382G>A	ENSP00000504193.1:n.*382G>A
ENST00000679267.1:n.3775G>A
ENST00000276079.12:c.*152G>A	ENSP00000276079.8:n.*152G>A
ENST00000373841.5:c.*152G>A	ENSP00000362947.1:n.*152G>A
ENST00000373856.7:c.*152G>A	ENSP00000362963.3:n.*152G>A
ENST00000472185.1:n.61-291G>A
ENST00000473525.1:n.1342G>A
ENST00000474431.5:n.603G>A
ENST00000490044.5:n.2275G>A
ENST00000535149.5:c.*152G>A	ENSP00000441364.1:n.*152G>A
NM_001145408.1:c.*152G>A	NP_001138880.1:n.*152G>A
NM_001145409.1:c.*152G>A	NP_001138881.1:n.*152G>A
NM_001145410.1:c.*152G>A	NP_001138882.1:n.*152G>A
NM_007363.4:c.*152G>A	NP_031389.3:n.*152G>A
NM_007363.5:c.*152G>A MANE Select	NP_031389.3:n.*152G>A
NM_001145408.2:c.*152G>A	NP_001138880.1:n.*152G>A
NM_001145409.2:c.*152G>A	NP_001138881.1:n.*152G>A
NM_001145410.2:c.*152G>A	NP_001138882.1:n.*152G>A