Canonical Allele Identifier: CA413550701

Gene: NONO

Linked Data

• MyVariant Identifiers: chrX:g.70519913G>C (hg19) ; chrX:g.71300063G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300063G>C , CM000685.2:g.71300063G>C	GRCh38
NC_000023.10:g.70519913G>C , CM000685.1:g.70519913G>C	GRCh37
NC_000023.9:g.70436638G>C	NCBI36
NG_046742.1:g.21872G>C
NG_054891.1:g.3789G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1403G>C MANE Select	ENSP00000276079.8:p.Arg468Pro
ENST00000373856.8:c.1501G>C	ENSP00000362963.4:p.Val501Leu
ENST00000420903.6:c.1403G>C	ENSP00000410299.2:p.Arg468Pro
ENST00000450092.6:c.1403G>C	ENSP00000415777.2:p.Arg468Pro
ENST00000454976.2:c.1403G>C	ENSP00000406673.2:p.Arg468Pro
ENST00000473525.2:n.2111G>C
ENST00000676495.1:n.2814G>C
ENST00000676499.1:n.2359G>C
ENST00000676797.1:c.1136G>C	ENSP00000503920.1:p.Arg379Pro
ENST00000677014.1:c.*1230G>C	ENSP00000503813.1:n.*1230G>C
ENST00000677218.1:n.2574G>C
ENST00000677245.1:c.*1612G>C	ENSP00000503929.1:n.*1612G>C
ENST00000677274.1:c.1403G>C	ENSP00000504314.1:p.Arg468Pro
ENST00000677446.1:c.1403G>C	ENSP00000503031.1:p.Arg468Pro
ENST00000677612.1:c.1403G>C	ENSP00000504351.1:p.Arg468Pro
ENST00000677766.1:n.3808G>C
ENST00000677826.1:n.2145G>C
ENST00000677879.1:c.1223G>C	ENSP00000504090.1:p.Arg408Pro
ENST00000677977.1:n.3235G>C
ENST00000678231.1:c.1403G>C	ENSP00000503233.1:p.Arg468Pro
ENST00000678323.1:n.2501G>C
ENST00000678335.1:c.*316G>C	ENSP00000503769.1:n.*316G>C
ENST00000678437.1:c.1394G>C	ENSP00000504007.1:p.Arg465Pro
ENST00000678660.1:c.1418G>C	ENSP00000504665.1:p.Arg473Pro
ENST00000678830.1:c.1493G>C	ENSP00000504263.1:p.Arg498Pro
ENST00000679029.1:c.*217G>C	ENSP00000504193.1:n.*217G>C
ENST00000679267.1:n.3610G>C
ENST00000276079.12:c.1403G>C	ENSP00000276079.8:p.Arg468Pro
ENST00000373841.5:c.1403G>C	ENSP00000362947.1:p.Arg468Pro
ENST00000373856.7:c.1403G>C	ENSP00000362963.3:p.Arg468Pro
ENST00000472185.1:n.61-456G>C
ENST00000473525.1:n.1177G>C
ENST00000474431.5:n.438G>C
ENST00000490044.5:n.2110G>C
ENST00000535149.5:c.1136G>C	ENSP00000441364.1:p.Arg379Pro
NM_001145408.1:c.1403G>C	NP_001138880.1:p.Arg468Pro
NM_001145409.1:c.1403G>C	NP_001138881.1:p.Arg468Pro
NM_001145410.1:c.1136G>C	NP_001138882.1:p.Arg379Pro
NM_007363.4:c.1403G>C	NP_031389.3:p.Arg468Pro
NM_007363.5:c.1403G>C MANE Select	NP_031389.3:p.Arg468Pro
NM_001145408.2:c.1403G>C	NP_001138880.1:p.Arg468Pro
NM_001145409.2:c.1403G>C	NP_001138881.1:p.Arg468Pro
NM_001145410.2:c.1136G>C	NP_001138882.1:p.Arg379Pro