Canonical Allele Identifier: CA2436414866

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300000_71300003delinsTTGG , CM000685.2:g.71300000_71300003delinsTTGG	GRCh38
NC_000023.10:g.70519850_70519853delinsTTGG , CM000685.1:g.70519850_70519853delinsTTGG	GRCh37
NC_000023.9:g.70436575_70436578delinsTTGG	NCBI36
NG_046742.1:g.21809_21812delinsTTGG
NG_054891.1:g.3726_3729delinsTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1340_1343delinsTTGG MANE Select	ENSP00000276079.8:p.Ile447=
ENST00000373856.8:c.1438_1441delinsTTGG	ENSP00000362963.4:p.Leu480=
ENST00000420903.6:c.1340_1343delinsTTGG	ENSP00000410299.2:p.Ile447=
ENST00000450092.6:c.1340_1343delinsTTGG	ENSP00000415777.2:p.Ile447=
ENST00000454976.2:c.1340_1343delinsTTGG	ENSP00000406673.2:p.Ile447=
ENST00000473525.2:n.2048_2051delinsTTGG
ENST00000676495.1:n.2751_2754delinsTTGG
ENST00000676499.1:n.2296_2299delinsTTGG
ENST00000676797.1:c.1073_1076delinsTTGG	ENSP00000503920.1:p.Ile358=
ENST00000677014.1:c.*1167_*1170delinsTTGG	ENSP00000503813.1:n.*1167_*1170delinsTTGG
ENST00000677218.1:n.2511_2514delinsTTGG
ENST00000677245.1:c.*1549_*1552delinsTTGG	ENSP00000503929.1:n.*1549_*1552delinsTTGG
ENST00000677274.1:c.1340_1343delinsTTGG	ENSP00000504314.1:p.Ile447=
ENST00000677446.1:c.1340_1343delinsTTGG	ENSP00000503031.1:p.Ile447=
ENST00000677612.1:c.1340_1343delinsTTGG	ENSP00000504351.1:p.Ile447=
ENST00000677766.1:n.3745_3748delinsTTGG
ENST00000677826.1:n.2082_2085delinsTTGG
ENST00000677879.1:c.1160_1163delinsTTGG	ENSP00000504090.1:p.Ile387=
ENST00000677977.1:n.3172_3175delinsTTGG
ENST00000678231.1:c.1340_1343delinsTTGG	ENSP00000503233.1:p.Ile447=
ENST00000678323.1:n.2438_2441delinsTTGG
ENST00000678335.1:c.*253_*256delinsTTGG	ENSP00000503769.1:n.*253_*256delinsTTGG
ENST00000678437.1:c.1331_1334delinsTTGG	ENSP00000504007.1:p.Ile444=
ENST00000678660.1:c.1355_1358delinsTTGG	ENSP00000504665.1:p.Ile452=
ENST00000678830.1:c.1430_1433delinsTTGG	ENSP00000504263.1:p.Ile477=
ENST00000679029.1:c.*154_*157delinsTTGG	ENSP00000504193.1:n.*154_*157delinsTTGG
ENST00000679267.1:n.3547_3550delinsTTGG
ENST00000276079.12:c.1340_1343delinsTTGG	ENSP00000276079.8:p.Ile447=
ENST00000373841.5:c.1340_1343delinsTTGG	ENSP00000362947.1:p.Ile447=
ENST00000373856.7:c.1340_1343delinsTTGG	ENSP00000362963.3:p.Ile447=
ENST00000472185.1:n.61-519_61-516delinsTTGG
ENST00000473525.1:n.1114_1117delinsTTGG
ENST00000474431.5:n.375_378delinsTTGG
ENST00000490044.5:n.2047_2050delinsTTGG
ENST00000535149.5:c.1073_1076delinsTTGG	ENSP00000441364.1:p.Ile358=
NM_001145408.1:c.1340_1343delinsTTGG	NP_001138880.1:p.Ile447=
NM_001145409.1:c.1340_1343delinsTTGG	NP_001138881.1:p.Ile447=
NM_001145410.1:c.1073_1076delinsTTGG	NP_001138882.1:p.Ile358=
NM_007363.4:c.1340_1343delinsTTGG	NP_031389.3:p.Ile447=
NM_007363.5:c.1340_1343delinsTTGG MANE Select	NP_031389.3:p.Ile447=
NM_001145408.2:c.1340_1343delinsTTGG	NP_001138880.1:p.Ile447=
NM_001145409.2:c.1340_1343delinsTTGG	NP_001138881.1:p.Ile447=
NM_001145410.2:c.1073_1076delinsTTGG	NP_001138882.1:p.Ile358=