Canonical Allele Identifier: CA877832005

Gene: NONO

Linked Data

• dbSNP Id: rs1202971562
• gnomAD v3: X-71300173-A-G
• gnomAD v4: X-71300173-A-G
• MyVariant Identifiers: chrX:g.70520023A>G (hg19) ; chrX:g.71300173A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300173A>G , CM000685.2:g.71300173A>G	GRCh38
NC_000023.10:g.70520023A>G , CM000685.1:g.70520023A>G	GRCh37
NC_000023.9:g.70436748A>G	NCBI36
NG_046742.1:g.21982A>G
NG_054891.1:g.3899A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*97A>G MANE Select	ENSP00000276079.8:n.*97A>G
ENST00000420903.6:c.*97A>G	ENSP00000410299.2:n.*97A>G
ENST00000473525.2:n.2221A>G
ENST00000676495.1:n.2924A>G
ENST00000676499.1:n.2469A>G
ENST00000676797.1:c.*97A>G	ENSP00000503920.1:n.*97A>G
ENST00000677014.1:c.*1340A>G	ENSP00000503813.1:n.*1340A>G
ENST00000677218.1:n.2684A>G
ENST00000677245.1:c.*1722A>G	ENSP00000503929.1:n.*1722A>G
ENST00000677274.1:c.*97A>G	ENSP00000504314.1:n.*97A>G
ENST00000677446.1:c.*97A>G	ENSP00000503031.1:n.*97A>G
ENST00000677612.1:c.*97A>G	ENSP00000504351.1:n.*97A>G
ENST00000677766.1:n.3918A>G
ENST00000677826.1:n.2255A>G
ENST00000677879.1:c.*97A>G	ENSP00000504090.1:n.*97A>G
ENST00000677977.1:n.3345A>G
ENST00000678231.1:c.*97A>G	ENSP00000503233.1:n.*97A>G
ENST00000678323.1:n.2611A>G
ENST00000678335.1:c.*426A>G	ENSP00000503769.1:n.*426A>G
ENST00000678437.1:c.*97A>G	ENSP00000504007.1:n.*97A>G
ENST00000678660.1:c.*97A>G	ENSP00000504665.1:n.*97A>G
ENST00000678830.1:c.*97A>G	ENSP00000504263.1:n.*97A>G
ENST00000679029.1:c.*327A>G	ENSP00000504193.1:n.*327A>G
ENST00000679267.1:n.3720A>G
ENST00000276079.12:c.*97A>G	ENSP00000276079.8:n.*97A>G
ENST00000373841.5:c.*97A>G	ENSP00000362947.1:n.*97A>G
ENST00000373856.7:c.*97A>G	ENSP00000362963.3:n.*97A>G
ENST00000472185.1:n.61-346A>G
ENST00000473525.1:n.1287A>G
ENST00000474431.5:n.548A>G
ENST00000490044.5:n.2220A>G
ENST00000535149.5:c.*97A>G	ENSP00000441364.1:n.*97A>G
NM_001145408.1:c.*97A>G	NP_001138880.1:n.*97A>G
NM_001145409.1:c.*97A>G	NP_001138881.1:n.*97A>G
NM_001145410.1:c.*97A>G	NP_001138882.1:n.*97A>G
NM_007363.4:c.*97A>G	NP_031389.3:n.*97A>G
NM_007363.5:c.*97A>G MANE Select	NP_031389.3:n.*97A>G
NM_001145408.2:c.*97A>G	NP_001138880.1:n.*97A>G
NM_001145409.2:c.*97A>G	NP_001138881.1:n.*97A>G
NM_001145410.2:c.*97A>G	NP_001138882.1:n.*97A>G