Canonical Allele Identifier: CA1931452168

Linked Data

dbSNP Id: rs2036465390

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99713488_99713489insTAAACAGATTAGAAATGTAACATACTCATTTAA , CM000672.2:g.99713488_99713489insTAAACAGATTAGAAATGTAACATACTCATTTAA GRCh38
NC_000010.10:g.101473245_101473246insTAAACAGATTAGAAATGTAACATACTCATTTAA , CM000672.1:g.101473245_101473246insTAAACAGATTAGAAATGTAACATACTCATTTAA GRCh37
NC_000010.9:g.101463235_101463236insTAAACAGATTAGAAATGTAACATACTCATTTAA NCBI36
NG_008986.1:g.24178_24179insTTAAATGAGTATGTTACATTTCTAATCTGTTTA , LRG_406:g.24178_24179insTTAAATGAGTATGTTACATTTCTAATCTGTTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000016171.6:c.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) MANE Select ENSP00000016171.6:n.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATC...
ENST00000649102.1:c.*460+2859_*460+2860insTTAAATGAGTATGTTACATTTCTAATCTGTTTA ENSP00000497114.1:n.*460+2859_*460+2860insTTAAATGAGTATGTTACAT...
ENST00000370483.9:c.1102-10_1102-9insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) ENSP00000359514.5:n.1102-10_1102-9insTTAAATGAGTATGTTACATTTCTA...
ENST00000493385.5:n.117-9430_117-9429insTAAACAGATTAGAAATGTAACATACTCATTTAA (CUTC)
NM_004376.5:c.1102-10_1102-9insTTAAATGAGTATGTTACATTTCTAATCTGTTTA , LRG_406t2:c.1102-10_1102-9insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_004367.2:n.1102-10_1102-9insTTAAATGAGTATGTTACATTTCTAATCTGT...
NM_078470.4:c.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGTTTA , LRG_406t1:c.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_510870.1:n.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGTTTA...
XM_005269539.3:c.1101+2859_1101+2860insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) XP_005269596.1:n.1101+2859_1101+2860insTTAAATGAGTATGTTACATTTC...
XM_006717633.2:c.*1279_*1280insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) XP_006717696.1:n.*1279_*1280insTTAAATGAGTATGTTACATTTCTAATCTGT...
XM_006717634.2:c.*49+2859_*49+2860insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) XP_006717697.1:n.*49+2859_*49+2860insTTAAATGAGTATGTTACATTTCTA...
XM_011539298.1:c.*50-10_*50-9insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) XP_011537600.1:n.*50-10_*50-9insTTAAATGAGTATGTTACATTTCTAATCTG...
NM_001320974.1:c.1101+2859_1101+2860insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_001307903.1:n.1101+2859_1101+2860insTTAAATGAGTATGTTACATTTC...
NM_001320975.1:c.*1279_*1280insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_001307904.1:n.*1279_*1280insTTAAATGAGTATGTTACATTTCTAATCTGT...
NM_001320976.1:c.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_001307905.1:n.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGT...
NM_004376.6:c.1102-10_1102-9insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_004367.2:n.1102-10_1102-9insTTAAATGAGTATGTTACATTTCTAATCTGT...
NM_078470.5:c.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_510870.1:n.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGTTTA...
XM_006717634.3:c.*49+2859_*49+2860insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) XP_006717697.1:n.*49+2859_*49+2860insTTAAATGAGTATGTTACATTTCTA...
XM_011539298.2:c.*50-10_*50-9insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) XP_011537600.1:n.*50-10_*50-9insTTAAATGAGTATGTTACATTTCTAATCTG...
NM_001320974.2:c.1101+2859_1101+2860insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_001307903.1:n.1101+2859_1101+2860insTTAAATGAGTATGTTACATTTC...
NM_001320975.2:c.*1279_*1280insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_001307904.1:n.*1279_*1280insTTAAATGAGTATGTTACATTTCTAATCTGT...
NM_001320976.2:c.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_001307905.1:n.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGT...
NM_001372024.1:c.*317_*318insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_001358953.1:n.*317_*318insTTAAATGAGTATGTTACATTTCTAATCTGTTT...
NM_001372025.1:c.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_001358954.1:n.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGT...
NM_001372026.1:c.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_001358955.1:n.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGT...
NM_001372027.1:c.*1202_*1203insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_001358956.1:n.*1202_*1203insTTAAATGAGTATGTTACATTTCTAATCTGT...
NM_001372028.1:c.*525_*526insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_001358957.1:n.*525_*526insTTAAATGAGTATGTTACATTTCTAATCTGTTT...
NM_004376.7:c.1102-10_1102-9insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) NP_004367.2:n.1102-10_1102-9insTTAAATGAGTATGTTACATTTCTAATCTGT...
NM_078470.6:c.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15) MANE Select NP_510870.1:n.*1098_*1099insTTAAATGAGTATGTTACATTTCTAATCTGTTTA...
NR_164009.1:n.2171_2172insTTAAATGAGTATGTTACATTTCTAATCTGTTTA (COX15)