Canonical Allele Identifier: CA331037185

Gene: NONO

Linked Data

• dbSNP Id: rs886215260
• gnomAD v2: X-70519936-G-C
• gnomAD v3: X-71300086-G-C
• gnomAD v4: X-71300086-G-C
• MyVariant Identifiers: chrX:g.70519936G>C (hg19) ; chrX:g.71300086G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300086G>C , CM000685.2:g.71300086G>C	GRCh38
NC_000023.10:g.70519936G>C , CM000685.1:g.70519936G>C	GRCh37
NC_000023.9:g.70436661G>C	NCBI36
NG_046742.1:g.21895G>C
NG_054891.1:g.3812G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*10G>C MANE Select	ENSP00000276079.8:n.*10G>C
ENST00000373856.8:c.1524G>C	ENSP00000362963.4:p.Gln508His
ENST00000420903.6:c.*10G>C	ENSP00000410299.2:n.*10G>C
ENST00000473525.2:n.2134G>C
ENST00000676495.1:n.2837G>C
ENST00000676499.1:n.2382G>C
ENST00000676797.1:c.*10G>C	ENSP00000503920.1:n.*10G>C
ENST00000677014.1:c.*1253G>C	ENSP00000503813.1:n.*1253G>C
ENST00000677218.1:n.2597G>C
ENST00000677245.1:c.*1635G>C	ENSP00000503929.1:n.*1635G>C
ENST00000677274.1:c.*10G>C	ENSP00000504314.1:n.*10G>C
ENST00000677446.1:c.*10G>C	ENSP00000503031.1:n.*10G>C
ENST00000677612.1:c.*10G>C	ENSP00000504351.1:n.*10G>C
ENST00000677766.1:n.3831G>C
ENST00000677826.1:n.2168G>C
ENST00000677879.1:c.*10G>C	ENSP00000504090.1:n.*10G>C
ENST00000677977.1:n.3258G>C
ENST00000678231.1:c.*10G>C	ENSP00000503233.1:n.*10G>C
ENST00000678323.1:n.2524G>C
ENST00000678335.1:c.*339G>C	ENSP00000503769.1:n.*339G>C
ENST00000678437.1:c.*10G>C	ENSP00000504007.1:n.*10G>C
ENST00000678660.1:c.*10G>C	ENSP00000504665.1:n.*10G>C
ENST00000678830.1:c.*10G>C	ENSP00000504263.1:n.*10G>C
ENST00000679029.1:c.*240G>C	ENSP00000504193.1:n.*240G>C
ENST00000679267.1:n.3633G>C
ENST00000276079.12:c.*10G>C	ENSP00000276079.8:n.*10G>C
ENST00000373841.5:c.*10G>C	ENSP00000362947.1:n.*10G>C
ENST00000373856.7:c.*10G>C	ENSP00000362963.3:n.*10G>C
ENST00000472185.1:n.61-433G>C
ENST00000473525.1:n.1200G>C
ENST00000474431.5:n.461G>C
ENST00000490044.5:n.2133G>C
ENST00000535149.5:c.*10G>C	ENSP00000441364.1:n.*10G>C
NM_001145408.1:c.*10G>C	NP_001138880.1:n.*10G>C
NM_001145409.1:c.*10G>C	NP_001138881.1:n.*10G>C
NM_001145410.1:c.*10G>C	NP_001138882.1:n.*10G>C
NM_007363.4:c.*10G>C	NP_031389.3:n.*10G>C
NM_007363.5:c.*10G>C MANE Select	NP_031389.3:n.*10G>C
NM_001145408.2:c.*10G>C	NP_001138880.1:n.*10G>C
NM_001145409.2:c.*10G>C	NP_001138881.1:n.*10G>C
NM_001145410.2:c.*10G>C	NP_001138882.1:n.*10G>C