Canonical Allele Identifier: CA877832042

Gene: NONO

Linked Data

• dbSNP Id: rs1466588543
• gnomAD v3: X-71300294-T-C
• gnomAD v4: X-71300294-T-C
• MyVariant Identifiers: chrX:g.70520144T>C (hg19) ; chrX:g.71300294T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300294T>C , CM000685.2:g.71300294T>C	GRCh38
NC_000023.10:g.70520144T>C , CM000685.1:g.70520144T>C	GRCh37
NC_000023.9:g.70436869T>C	NCBI36
NG_046742.1:g.22103T>C
NG_054891.1:g.4020T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*218T>C MANE Select	ENSP00000276079.8:n.*218T>C
ENST00000420903.6:c.*218T>C	ENSP00000410299.2:n.*218T>C
ENST00000473525.2:n.2342T>C
ENST00000676495.1:n.3045T>C
ENST00000676499.1:n.2590T>C
ENST00000676797.1:c.*218T>C	ENSP00000503920.1:n.*218T>C
ENST00000677014.1:c.*1461T>C	ENSP00000503813.1:n.*1461T>C
ENST00000677218.1:n.2805T>C
ENST00000677245.1:c.*1843T>C	ENSP00000503929.1:n.*1843T>C
ENST00000677274.1:c.*218T>C	ENSP00000504314.1:n.*218T>C
ENST00000677446.1:c.*218T>C	ENSP00000503031.1:n.*218T>C
ENST00000677612.1:c.*218T>C	ENSP00000504351.1:n.*218T>C
ENST00000677766.1:n.4039T>C
ENST00000677826.1:n.2376T>C
ENST00000677879.1:c.*218T>C	ENSP00000504090.1:n.*218T>C
ENST00000677977.1:n.3466T>C
ENST00000678231.1:c.*218T>C	ENSP00000503233.1:n.*218T>C
ENST00000678323.1:n.2732T>C
ENST00000678335.1:c.*547T>C	ENSP00000503769.1:n.*547T>C
ENST00000678437.1:c.*218T>C	ENSP00000504007.1:n.*218T>C
ENST00000678660.1:c.*218T>C	ENSP00000504665.1:n.*218T>C
ENST00000678830.1:c.*218T>C	ENSP00000504263.1:n.*218T>C
ENST00000679029.1:c.*448T>C	ENSP00000504193.1:n.*448T>C
ENST00000679267.1:n.3841T>C
ENST00000276079.12:c.*218T>C	ENSP00000276079.8:n.*218T>C
ENST00000373841.5:c.*218T>C	ENSP00000362947.1:n.*218T>C
ENST00000472185.1:n.61-225T>C
ENST00000473525.1:n.1408T>C
ENST00000490044.5:n.2341T>C
ENST00000535149.5:c.*218T>C	ENSP00000441364.1:n.*218T>C
NM_001145408.1:c.*218T>C	NP_001138880.1:n.*218T>C
NM_001145409.1:c.*218T>C	NP_001138881.1:n.*218T>C
NM_001145410.1:c.*218T>C	NP_001138882.1:n.*218T>C
NM_007363.4:c.*218T>C	NP_031389.3:n.*218T>C
NM_007363.5:c.*218T>C MANE Select	NP_031389.3:n.*218T>C
NM_001145408.2:c.*218T>C	NP_001138880.1:n.*218T>C
NM_001145409.2:c.*218T>C	NP_001138881.1:n.*218T>C
NM_001145410.2:c.*218T>C	NP_001138882.1:n.*218T>C