Canonical Allele Identifier: CA1931452293

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713686_99713701delinsCTAGCTGGGCGTGGTG , CM000672.2:g.99713686_99713701delinsCTAGCTGGGCGTGGTG	GRCh38
NC_000010.10:g.101473443_101473458delinsCTAGCTGGGCGTGGTG , CM000672.1:g.101473443_101473458delinsCTAGCTGGGCGTGGTG	GRCh37
NC_000010.9:g.101463433_101463448delinsCTAGCTGGGCGTGGTG	NCBI36
NG_008986.1:g.23966_23981delinsCACCACGCCCAGCTAG , LRG_406:g.23966_23981delinsCACCACGCCCAGCTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*886_*901delinsCACCACGCCCAGCTAG (COX15) MANE Select	ENSP00000016171.6:n.*886_*901delinsCACCACGCCCAGCTAG
ENST00000649102.1:c.*460+2647_*460+2662delinsCACCACGCCCAGCTAG	ENSP00000497114.1:n.*460+2647_*460+2662delinsCACCACGCCCAGCTAG...
ENST00000016171.5:c.*886_*901delinsCACCACGCCCAGCTAG (COX15)	ENSP00000016171.5:n.*886_*901delinsCACCACGCCCAGCTAG
ENST00000370483.9:c.1102-222_1102-207delinsCACCACGCCCAGCTAG (COX15)	ENSP00000359514.5:n.1102-222_1102-207delinsCACCACGCCCAGCTAG
ENST00000493385.5:n.117-9232_117-9217delinsCTAGCTGGGCGTGGTG (CUTC)
NM_004376.5:c.1102-222_1102-207delinsCACCACGCCCAGCTAG , LRG_406t2:c.1102-222_1102-207delinsCACCACGCCCAGCTAG (COX15)	NP_004367.2:n.1102-222_1102-207delinsCACCACGCCCAGCTAG
NM_078470.4:c.*886_*901delinsCACCACGCCCAGCTAG , LRG_406t1:c.*886_*901delinsCACCACGCCCAGCTAG (COX15)	NP_510870.1:n.*886_*901delinsCACCACGCCCAGCTAG
XM_005269539.3:c.1101+2647_1101+2662delinsCACCACGCCCAGCTAG (COX15)	XP_005269596.1:n.1101+2647_1101+2662delinsCACCACGCCCAGCTAG
XM_006717633.2:c.*1067_*1082delinsCACCACGCCCAGCTAG (COX15)	XP_006717696.1:n.*1067_*1082delinsCACCACGCCCAGCTAG
XM_006717634.2:c.*49+2647_*49+2662delinsCACCACGCCCAGCTAG (COX15)	XP_006717697.1:n.*49+2647_*49+2662delinsCACCACGCCCAGCTAG
XM_011539298.1:c.*50-222_*50-207delinsCACCACGCCCAGCTAG (COX15)	XP_011537600.1:n.*50-222_*50-207delinsCACCACGCCCAGCTAG
NM_001320974.1:c.1101+2647_1101+2662delinsCACCACGCCCAGCTAG (COX15)	NP_001307903.1:n.1101+2647_1101+2662delinsCACCACGCCCAGCTAG
NM_001320975.1:c.*1067_*1082delinsCACCACGCCCAGCTAG (COX15)	NP_001307904.1:n.*1067_*1082delinsCACCACGCCCAGCTAG
NM_001320976.1:c.*886_*901delinsCACCACGCCCAGCTAG (COX15)	NP_001307905.1:n.*886_*901delinsCACCACGCCCAGCTAG
NM_004376.6:c.1102-222_1102-207delinsCACCACGCCCAGCTAG (COX15)	NP_004367.2:n.1102-222_1102-207delinsCACCACGCCCAGCTAG
NM_078470.5:c.*886_*901delinsCACCACGCCCAGCTAG (COX15)	NP_510870.1:n.*886_*901delinsCACCACGCCCAGCTAG
XM_006717634.3:c.*49+2647_*49+2662delinsCACCACGCCCAGCTAG (COX15)	XP_006717697.1:n.*49+2647_*49+2662delinsCACCACGCCCAGCTAG
XM_011539298.2:c.*50-222_*50-207delinsCACCACGCCCAGCTAG (COX15)	XP_011537600.1:n.*50-222_*50-207delinsCACCACGCCCAGCTAG
NM_001320974.2:c.1101+2647_1101+2662delinsCACCACGCCCAGCTAG (COX15)	NP_001307903.1:n.1101+2647_1101+2662delinsCACCACGCCCAGCTAG
NM_001320975.2:c.*1067_*1082delinsCACCACGCCCAGCTAG (COX15)	NP_001307904.1:n.*1067_*1082delinsCACCACGCCCAGCTAG
NM_001320976.2:c.*886_*901delinsCACCACGCCCAGCTAG (COX15)	NP_001307905.1:n.*886_*901delinsCACCACGCCCAGCTAG
NM_001372024.1:c.*105_*120delinsCACCACGCCCAGCTAG (COX15)	NP_001358953.1:n.*105_*120delinsCACCACGCCCAGCTAG
NM_001372025.1:c.*886_*901delinsCACCACGCCCAGCTAG (COX15)	NP_001358954.1:n.*886_*901delinsCACCACGCCCAGCTAG
NM_001372026.1:c.*886_*901delinsCACCACGCCCAGCTAG (COX15)	NP_001358955.1:n.*886_*901delinsCACCACGCCCAGCTAG
NM_001372027.1:c.*990_*1005delinsCACCACGCCCAGCTAG (COX15)	NP_001358956.1:n.*990_*1005delinsCACCACGCCCAGCTAG
NM_001372028.1:c.*313_*328delinsCACCACGCCCAGCTAG (COX15)	NP_001358957.1:n.*313_*328delinsCACCACGCCCAGCTAG
NM_004376.7:c.1102-222_1102-207delinsCACCACGCCCAGCTAG (COX15)	NP_004367.2:n.1102-222_1102-207delinsCACCACGCCCAGCTAG
NM_078470.6:c.*886_*901delinsCACCACGCCCAGCTAG (COX15) MANE Select	NP_510870.1:n.*886_*901delinsCACCACGCCCAGCTAG
NR_164009.1:n.1959_1974delinsCACCACGCCCAGCTAG (COX15)