Canonical Allele Identifier: CA2526680865

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713606_99713607insTGGCCTTATAT , CM000672.2:g.99713606_99713607insTGGCCTTATAT	GRCh38
NC_000010.10:g.101473363_101473364insTGGCCTTATAT , CM000672.1:g.101473363_101473364insTGGCCTTATAT	GRCh37
NC_000010.9:g.101463353_101463354insTGGCCTTATAT	NCBI36
NG_008986.1:g.24060_24061insATATAAGGCCA , LRG_406:g.24060_24061insATATAAGGCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*980_*981insATATAAGGCCA (COX15) MANE Select	ENSP00000016171.6:n.*980_*981insATATAAGGCCA
ENST00000649102.1:c.*460+2741_*460+2742insATATAAGGCCA	ENSP00000497114.1:n.*460+2741_*460+2742insATATAAGGCCA
ENST00000016171.5:c.*980_*981insATATAAGGCCA (COX15)	ENSP00000016171.5:n.*980_*981insATATAAGGCCA
ENST00000370483.9:c.1102-128_1102-127insATATAAGGCCA (COX15)	ENSP00000359514.5:n.1102-128_1102-127insATATAAGGCCA
ENST00000493385.5:n.117-9312_117-9311insTGGCCTTATAT (CUTC)
NM_004376.5:c.1102-128_1102-127insATATAAGGCCA , LRG_406t2:c.1102-128_1102-127insATATAAGGCCA (COX15)	NP_004367.2:n.1102-128_1102-127insATATAAGGCCA
NM_078470.4:c.*980_*981insATATAAGGCCA , LRG_406t1:c.*980_*981insATATAAGGCCA (COX15)	NP_510870.1:n.*980_*981insATATAAGGCCA
XM_005269539.3:c.1101+2741_1101+2742insATATAAGGCCA (COX15)	XP_005269596.1:n.1101+2741_1101+2742insATATAAGGCCA
XM_006717633.2:c.*1161_*1162insATATAAGGCCA (COX15)	XP_006717696.1:n.*1161_*1162insATATAAGGCCA
XM_006717634.2:c.*49+2741_*49+2742insATATAAGGCCA (COX15)	XP_006717697.1:n.*49+2741_*49+2742insATATAAGGCCA
XM_011539298.1:c.*50-128_*50-127insATATAAGGCCA (COX15)	XP_011537600.1:n.*50-128_*50-127insATATAAGGCCA
NM_001320974.1:c.1101+2741_1101+2742insATATAAGGCCA (COX15)	NP_001307903.1:n.1101+2741_1101+2742insATATAAGGCCA
NM_001320975.1:c.*1161_*1162insATATAAGGCCA (COX15)	NP_001307904.1:n.*1161_*1162insATATAAGGCCA
NM_001320976.1:c.*980_*981insATATAAGGCCA (COX15)	NP_001307905.1:n.*980_*981insATATAAGGCCA
NM_004376.6:c.1102-128_1102-127insATATAAGGCCA (COX15)	NP_004367.2:n.1102-128_1102-127insATATAAGGCCA
NM_078470.5:c.*980_*981insATATAAGGCCA (COX15)	NP_510870.1:n.*980_*981insATATAAGGCCA
XM_006717634.3:c.*49+2741_*49+2742insATATAAGGCCA (COX15)	XP_006717697.1:n.*49+2741_*49+2742insATATAAGGCCA
XM_011539298.2:c.*50-128_*50-127insATATAAGGCCA (COX15)	XP_011537600.1:n.*50-128_*50-127insATATAAGGCCA
NM_001320974.2:c.1101+2741_1101+2742insATATAAGGCCA (COX15)	NP_001307903.1:n.1101+2741_1101+2742insATATAAGGCCA
NM_001320975.2:c.*1161_*1162insATATAAGGCCA (COX15)	NP_001307904.1:n.*1161_*1162insATATAAGGCCA
NM_001320976.2:c.*980_*981insATATAAGGCCA (COX15)	NP_001307905.1:n.*980_*981insATATAAGGCCA
NM_001372024.1:c.*199_*200insATATAAGGCCA (COX15)	NP_001358953.1:n.*199_*200insATATAAGGCCA
NM_001372025.1:c.*980_*981insATATAAGGCCA (COX15)	NP_001358954.1:n.*980_*981insATATAAGGCCA
NM_001372026.1:c.*980_*981insATATAAGGCCA (COX15)	NP_001358955.1:n.*980_*981insATATAAGGCCA
NM_001372027.1:c.*1084_*1085insATATAAGGCCA (COX15)	NP_001358956.1:n.*1084_*1085insATATAAGGCCA
NM_001372028.1:c.*407_*408insATATAAGGCCA (COX15)	NP_001358957.1:n.*407_*408insATATAAGGCCA
NM_004376.7:c.1102-128_1102-127insATATAAGGCCA (COX15)	NP_004367.2:n.1102-128_1102-127insATATAAGGCCA
NM_078470.6:c.*980_*981insATATAAGGCCA (COX15) MANE Select	NP_510870.1:n.*980_*981insATATAAGGCCA
NR_164009.1:n.2053_2054insATATAAGGCCA (COX15)