Canonical Allele Identifier: CA1931452128

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713448_99713449delinsAT , CM000672.2:g.99713448_99713449delinsAT	GRCh38
NC_000010.10:g.101473205_101473206delinsAT , CM000672.1:g.101473205_101473206delinsAT	GRCh37
NC_000010.9:g.101463195_101463196delinsAT	NCBI36
NG_008986.1:g.24218_24219delinsAT , LRG_406:g.24218_24219delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*1138_*1139delinsAT (COX15) MANE Select	ENSP00000016171.6:n.*1138_*1139delinsAT
ENST00000649102.1:c.*460+2899_*460+2900delinsAT	ENSP00000497114.1:n.*460+2899_*460+2900delinsAT
ENST00000370483.9:c.1132_1133delinsAT (COX15)	ENSP00000359514.5:p.Ile378=
ENST00000493385.5:n.117-9470_117-9469delinsAT (CUTC)
NM_004376.5:c.1132_1133delinsAT , LRG_406t2:c.1132_1133delinsAT (COX15)	NP_004367.2:p.Ile378=
NM_078470.4:c.*1138_*1139delinsAT , LRG_406t1:c.*1138_*1139delinsAT (COX15)	NP_510870.1:n.*1138_*1139delinsAT
XM_005269539.3:c.1101+2899_1101+2900delinsAT (COX15)	XP_005269596.1:n.1101+2899_1101+2900delinsAT
XM_006717633.2:c.*1319_*1320delinsAT (COX15)	XP_006717696.1:n.*1319_*1320delinsAT
XM_006717634.2:c.*49+2899_*49+2900delinsAT (COX15)	XP_006717697.1:n.*49+2899_*49+2900delinsAT
XM_011539298.1:c.*80_*81delinsAT (COX15)	XP_011537600.1:n.*80_*81delinsAT
NM_001320974.1:c.1101+2899_1101+2900delinsAT (COX15)	NP_001307903.1:n.1101+2899_1101+2900delinsAT
NM_001320975.1:c.*1319_*1320delinsAT (COX15)	NP_001307904.1:n.*1319_*1320delinsAT
NM_001320976.1:c.*1138_*1139delinsAT (COX15)	NP_001307905.1:n.*1138_*1139delinsAT
NM_004376.6:c.1132_1133delinsAT (COX15)	NP_004367.2:p.Ile378=
NM_078470.5:c.*1138_*1139delinsAT (COX15)	NP_510870.1:n.*1138_*1139delinsAT
XM_006717634.3:c.*49+2899_*49+2900delinsAT (COX15)	XP_006717697.1:n.*49+2899_*49+2900delinsAT
XM_011539298.2:c.*80_*81delinsAT (COX15)	XP_011537600.1:n.*80_*81delinsAT
NM_001320974.2:c.1101+2899_1101+2900delinsAT (COX15)	NP_001307903.1:n.1101+2899_1101+2900delinsAT
NM_001320975.2:c.*1319_*1320delinsAT (COX15)	NP_001307904.1:n.*1319_*1320delinsAT
NM_001320976.2:c.*1138_*1139delinsAT (COX15)	NP_001307905.1:n.*1138_*1139delinsAT
NM_001372024.1:c.*357_*358delinsAT (COX15)	NP_001358953.1:n.*357_*358delinsAT
NM_001372025.1:c.*1138_*1139delinsAT (COX15)	NP_001358954.1:n.*1138_*1139delinsAT
NM_001372026.1:c.*1138_*1139delinsAT (COX15)	NP_001358955.1:n.*1138_*1139delinsAT
NM_001372027.1:c.*1242_*1243delinsAT (COX15)	NP_001358956.1:n.*1242_*1243delinsAT
NM_001372028.1:c.*565_*566delinsAT (COX15)	NP_001358957.1:n.*565_*566delinsAT
NM_004376.7:c.1132_1133delinsAT (COX15)	NP_004367.2:p.Ile378=
NM_078470.6:c.*1138_*1139delinsAT (COX15) MANE Select	NP_510870.1:n.*1138_*1139delinsAT
NR_164009.1:n.2211_2212delinsAT (COX15)