Canonical Allele Identifier: CA2579641018

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300111_71300112del , CM000685.2:g.71300111_71300112del	GRCh38
NC_000023.10:g.70519961_70519962del , CM000685.1:g.70519961_70519962del	GRCh37
NC_000023.9:g.70436686_70436687del	NCBI36
NG_046742.1:g.21920_21921del
NG_054891.1:g.3837_3838del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*35_*36del MANE Select	ENSP00000276079.8:n.*35_*36del
ENST00000420903.6:c.*35_*36del	ENSP00000410299.2:n.*35_*36del
ENST00000473525.2:n.2159_2160del
ENST00000676495.1:n.2862_2863del
ENST00000676499.1:n.2407_2408del
ENST00000676797.1:c.*35_*36del	ENSP00000503920.1:n.*35_*36del
ENST00000677014.1:c.*1278_*1279del	ENSP00000503813.1:n.*1278_*1279del
ENST00000677218.1:n.2622_2623del
ENST00000677245.1:c.*1660_*1661del	ENSP00000503929.1:n.*1660_*1661del
ENST00000677274.1:c.*35_*36del	ENSP00000504314.1:n.*35_*36del
ENST00000677446.1:c.*35_*36del	ENSP00000503031.1:n.*35_*36del
ENST00000677612.1:c.*35_*36del	ENSP00000504351.1:n.*35_*36del
ENST00000677766.1:n.3856_3857del
ENST00000677826.1:n.2193_2194del
ENST00000677879.1:c.*35_*36del	ENSP00000504090.1:n.*35_*36del
ENST00000677977.1:n.3283_3284del
ENST00000678231.1:c.*35_*36del	ENSP00000503233.1:n.*35_*36del
ENST00000678323.1:n.2549_2550del
ENST00000678335.1:c.*364_*365del	ENSP00000503769.1:n.*364_*365del
ENST00000678437.1:c.*35_*36del	ENSP00000504007.1:n.*35_*36del
ENST00000678660.1:c.*35_*36del	ENSP00000504665.1:n.*35_*36del
ENST00000678830.1:c.*35_*36del	ENSP00000504263.1:n.*35_*36del
ENST00000679029.1:c.*265_*266del	ENSP00000504193.1:n.*265_*266del
ENST00000679267.1:n.3658_3659del
ENST00000276079.12:c.*35_*36del	ENSP00000276079.8:n.*35_*36del
ENST00000373841.5:c.*35_*36del	ENSP00000362947.1:n.*35_*36del
ENST00000373856.7:c.*35_*36del	ENSP00000362963.3:n.*35_*36del
ENST00000472185.1:n.61-408_61-407del
ENST00000473525.1:n.1225_1226del
ENST00000474431.5:n.486_487del
ENST00000490044.5:n.2158_2159del
ENST00000535149.5:c.*35_*36del	ENSP00000441364.1:n.*35_*36del
NM_001145408.1:c.*35_*36del	NP_001138880.1:n.*35_*36del
NM_001145409.1:c.*35_*36del	NP_001138881.1:n.*35_*36del
NM_001145410.1:c.*35_*36del	NP_001138882.1:n.*35_*36del
NM_007363.4:c.*35_*36del	NP_031389.3:n.*35_*36del
NM_007363.5:c.*35_*36del MANE Select	NP_031389.3:n.*35_*36del
NM_001145408.2:c.*35_*36del	NP_001138880.1:n.*35_*36del
NM_001145409.2:c.*35_*36del	NP_001138881.1:n.*35_*36del
NM_001145410.2:c.*35_*36del	NP_001138882.1:n.*35_*36del