Canonical Allele Identifier: CA2789195170

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713799_99713800insGG , CM000672.2:g.99713799_99713800insGG	GRCh38
NC_000010.10:g.101473556_101473557insGG , CM000672.1:g.101473556_101473557insGG	GRCh37
NC_000010.9:g.101463546_101463547insGG	NCBI36
NG_008986.1:g.23867_23868insCC , LRG_406:g.23867_23868insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*787_*788insCC (COX15) MANE Select	ENSP00000016171.6:n.*787_*788insCC
ENST00000649102.1:c.*460+2548_*460+2549insCC	ENSP00000497114.1:n.*460+2548_*460+2549insCC
ENST00000016171.5:c.*787_*788insCC (COX15)	ENSP00000016171.5:n.*787_*788insCC
ENST00000370483.9:c.1102-321_1102-320insCC (COX15)	ENSP00000359514.5:n.1102-321_1102-320insCC
ENST00000493385.5:n.117-9119_117-9118insGG (CUTC)
NM_004376.5:c.1102-321_1102-320insCC , LRG_406t2:c.1102-321_1102-320insCC (COX15)	NP_004367.2:n.1102-321_1102-320insCC
NM_078470.4:c.*787_*788insCC , LRG_406t1:c.*787_*788insCC (COX15)	NP_510870.1:n.*787_*788insCC
XM_005269539.3:c.1101+2548_1101+2549insCC (COX15)	XP_005269596.1:n.1101+2548_1101+2549insCC
XM_006717633.2:c.*968_*969insCC (COX15)	XP_006717696.1:n.*968_*969insCC
XM_006717634.2:c.*49+2548_*49+2549insCC (COX15)	XP_006717697.1:n.*49+2548_*49+2549insCC
XM_011539298.1:c.*50-321_*50-320insCC (COX15)	XP_011537600.1:n.*50-321_*50-320insCC
NM_001320974.1:c.1101+2548_1101+2549insCC (COX15)	NP_001307903.1:n.1101+2548_1101+2549insCC
NM_001320975.1:c.*968_*969insCC (COX15)	NP_001307904.1:n.*968_*969insCC
NM_001320976.1:c.*787_*788insCC (COX15)	NP_001307905.1:n.*787_*788insCC
NM_004376.6:c.1102-321_1102-320insCC (COX15)	NP_004367.2:n.1102-321_1102-320insCC
NM_078470.5:c.*787_*788insCC (COX15)	NP_510870.1:n.*787_*788insCC
XM_006717634.3:c.*49+2548_*49+2549insCC (COX15)	XP_006717697.1:n.*49+2548_*49+2549insCC
XM_011539298.2:c.*50-321_*50-320insCC (COX15)	XP_011537600.1:n.*50-321_*50-320insCC
NM_001320974.2:c.1101+2548_1101+2549insCC (COX15)	NP_001307903.1:n.1101+2548_1101+2549insCC
NM_001320975.2:c.*968_*969insCC (COX15)	NP_001307904.1:n.*968_*969insCC
NM_001320976.2:c.*787_*788insCC (COX15)	NP_001307905.1:n.*787_*788insCC
NM_001372024.1:c.*6_*7insCC (COX15)	NP_001358953.1:n.*6_*7insCC
NM_001372025.1:c.*787_*788insCC (COX15)	NP_001358954.1:n.*787_*788insCC
NM_001372026.1:c.*787_*788insCC (COX15)	NP_001358955.1:n.*787_*788insCC
NM_001372027.1:c.*891_*892insCC (COX15)	NP_001358956.1:n.*891_*892insCC
NM_001372028.1:c.*214_*215insCC (COX15)	NP_001358957.1:n.*214_*215insCC
NM_004376.7:c.1102-321_1102-320insCC (COX15)	NP_004367.2:n.1102-321_1102-320insCC
NM_078470.6:c.*787_*788insCC (COX15) MANE Select	NP_510870.1:n.*787_*788insCC
NR_164009.1:n.1860_1861insCC (COX15)