Canonical Allele Identifier: CA2557452841

Gene: NONO

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300057_71300164del , CM000685.2:g.71300057_71300164del	GRCh38
NC_000023.10:g.70519907_70520014del , CM000685.1:g.70519907_70520014del	GRCh37
NC_000023.9:g.70436632_70436739del	NCBI36
NG_046742.1:g.21866_21973del
NG_054891.1:g.3783_3890del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1397_*88del MANE Select	ENSP00000276079.8:n.[c.1397_*88del;Asn466IlefsTer6]
ENST00000420903.6:c.1397_*88del	ENSP00000410299.2:n.[c.1397_*88del;Asn466IlefsTer6]
ENST00000473525.2:n.2105_2212del
ENST00000676495.1:n.2808_2915del
ENST00000676499.1:n.2353_2460del
ENST00000676797.1:c.1130_*88del	ENSP00000503920.1:n.[c.1130_*88del;Asn377IlefsTer6]
ENST00000677014.1:c.*1224_*1331del	ENSP00000503813.1:n.*1224_*1331del
ENST00000677218.1:n.2568_2675del
ENST00000677245.1:c.*1606_*1713del	ENSP00000503929.1:n.*1606_*1713del
ENST00000677274.1:c.1397_*88del	ENSP00000504314.1:n.[c.1397_*88del;Asn466IlefsTer6]
ENST00000677446.1:c.1397_*88del	ENSP00000503031.1:n.[c.1397_*88del;Asn466IlefsTer6]
ENST00000677612.1:c.1397_*88del	ENSP00000504351.1:n.[c.1397_*88del;Asn466IlefsTer6]
ENST00000677766.1:n.3802_3909del
ENST00000677826.1:n.2139_2246del
ENST00000677879.1:c.1217_*88del	ENSP00000504090.1:n.[c.1217_*88del;Asn406IlefsTer6]
ENST00000677977.1:n.3229_3336del
ENST00000678231.1:c.1397_*88del	ENSP00000503233.1:n.[c.1397_*88del;Asn466IlefsTer6]
ENST00000678323.1:n.2495_2602del
ENST00000678335.1:c.*310_*417del	ENSP00000503769.1:n.*310_*417del
ENST00000678437.1:c.1388_*88del	ENSP00000504007.1:n.[c.1388_*88del;Asn463IlefsTer6]
ENST00000678660.1:c.1412_*88del	ENSP00000504665.1:n.[c.1412_*88del;Asn471IlefsTer6]
ENST00000678830.1:c.1487_*88del	ENSP00000504263.1:n.[c.1487_*88del;Asn496IlefsTer6]
ENST00000679029.1:c.*211_*318del	ENSP00000504193.1:n.*211_*318del
ENST00000679267.1:n.3604_3711del
ENST00000276079.12:c.1397_*88del	ENSP00000276079.8:n.[c.1397_*88del;Asn466IlefsTer6]
ENST00000373841.5:c.1397_*88del	ENSP00000362947.1:n.[c.1397_*88del;Asn466IlefsTer6]
ENST00000373856.7:c.1397_*88del	ENSP00000362963.3:n.[c.1397_*88del;Asn466IlefsTer6]
ENST00000472185.1:n.61-462_61-355del
ENST00000473525.1:n.1171_1278del
ENST00000474431.5:n.432_539del
ENST00000490044.5:n.2104_2211del
ENST00000535149.5:c.1130_*88del	ENSP00000441364.1:n.[c.1130_*88del;Asn377IlefsTer6]
NM_001145408.1:c.1397_*88del	NP_001138880.1:n.[c.1397_*88del;Asn466IlefsTer6]
NM_001145409.1:c.1397_*88del	NP_001138881.1:n.[c.1397_*88del;Asn466IlefsTer6]
NM_001145410.1:c.1130_*88del	NP_001138882.1:n.[c.1130_*88del;Asn377IlefsTer6]
NM_007363.4:c.1397_*88del	NP_031389.3:n.[c.1397_*88del;Asn466IlefsTer6]
NM_007363.5:c.1397_*88del MANE Select	NP_031389.3:n.[c.1397_*88del;Asn466IlefsTer6]
NM_001145408.2:c.1397_*88del	NP_001138880.1:n.[c.1397_*88del;Asn466IlefsTer6]
NM_001145409.2:c.1397_*88del	NP_001138881.1:n.[c.1397_*88del;Asn466IlefsTer6]
NM_001145410.2:c.1130_*88del	NP_001138882.1:n.[c.1130_*88del;Asn377IlefsTer6]