Canonical Allele Identifier: CA1931452360

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713775_99713776delinsGC , CM000672.2:g.99713775_99713776delinsGC	GRCh38
NC_000010.10:g.101473532_101473533delinsGC , CM000672.1:g.101473532_101473533delinsGC	GRCh37
NC_000010.9:g.101463522_101463523delinsGC	NCBI36
NG_008986.1:g.23891_23892delinsGC , LRG_406:g.23891_23892delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*811_*812delinsGC (COX15) MANE Select	ENSP00000016171.6:n.*811_*812delinsGC
ENST00000649102.1:c.*460+2572_*460+2573delinsGC	ENSP00000497114.1:n.*460+2572_*460+2573delinsGC
ENST00000016171.5:c.*811_*812delinsGC (COX15)	ENSP00000016171.5:n.*811_*812delinsGC
ENST00000370483.9:c.1102-297_1102-296delinsGC (COX15)	ENSP00000359514.5:n.1102-297_1102-296delinsGC
ENST00000493385.5:n.117-9143_117-9142delinsGC (CUTC)
NM_004376.5:c.1102-297_1102-296delinsGC , LRG_406t2:c.1102-297_1102-296delinsGC (COX15)	NP_004367.2:n.1102-297_1102-296delinsGC
NM_078470.4:c.*811_*812delinsGC , LRG_406t1:c.*811_*812delinsGC (COX15)	NP_510870.1:n.*811_*812delinsGC
XM_005269539.3:c.1101+2572_1101+2573delinsGC (COX15)	XP_005269596.1:n.1101+2572_1101+2573delinsGC
XM_006717633.2:c.*992_*993delinsGC (COX15)	XP_006717696.1:n.*992_*993delinsGC
XM_006717634.2:c.*49+2572_*49+2573delinsGC (COX15)	XP_006717697.1:n.*49+2572_*49+2573delinsGC
XM_011539298.1:c.*50-297_*50-296delinsGC (COX15)	XP_011537600.1:n.*50-297_*50-296delinsGC
NM_001320974.1:c.1101+2572_1101+2573delinsGC (COX15)	NP_001307903.1:n.1101+2572_1101+2573delinsGC
NM_001320975.1:c.*992_*993delinsGC (COX15)	NP_001307904.1:n.*992_*993delinsGC
NM_001320976.1:c.*811_*812delinsGC (COX15)	NP_001307905.1:n.*811_*812delinsGC
NM_004376.6:c.1102-297_1102-296delinsGC (COX15)	NP_004367.2:n.1102-297_1102-296delinsGC
NM_078470.5:c.*811_*812delinsGC (COX15)	NP_510870.1:n.*811_*812delinsGC
XM_006717634.3:c.*49+2572_*49+2573delinsGC (COX15)	XP_006717697.1:n.*49+2572_*49+2573delinsGC
XM_011539298.2:c.*50-297_*50-296delinsGC (COX15)	XP_011537600.1:n.*50-297_*50-296delinsGC
NM_001320974.2:c.1101+2572_1101+2573delinsGC (COX15)	NP_001307903.1:n.1101+2572_1101+2573delinsGC
NM_001320975.2:c.*992_*993delinsGC (COX15)	NP_001307904.1:n.*992_*993delinsGC
NM_001320976.2:c.*811_*812delinsGC (COX15)	NP_001307905.1:n.*811_*812delinsGC
NM_001372024.1:c.*30_*31delinsGC (COX15)	NP_001358953.1:n.*30_*31delinsGC
NM_001372025.1:c.*811_*812delinsGC (COX15)	NP_001358954.1:n.*811_*812delinsGC
NM_001372026.1:c.*811_*812delinsGC (COX15)	NP_001358955.1:n.*811_*812delinsGC
NM_001372027.1:c.*915_*916delinsGC (COX15)	NP_001358956.1:n.*915_*916delinsGC
NM_001372028.1:c.*238_*239delinsGC (COX15)	NP_001358957.1:n.*238_*239delinsGC
NM_004376.7:c.1102-297_1102-296delinsGC (COX15)	NP_004367.2:n.1102-297_1102-296delinsGC
NM_078470.6:c.*811_*812delinsGC (COX15) MANE Select	NP_510870.1:n.*811_*812delinsGC
NR_164009.1:n.1884_1885delinsGC (COX15)