Canonical Allele Identifier: CA1931452218

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713576_99713581delinsATTTTT , CM000672.2:g.99713576_99713581delinsATTTTT	GRCh38
NC_000010.10:g.101473333_101473338delinsATTTTT , CM000672.1:g.101473333_101473338delinsATTTTT	GRCh37
NC_000010.9:g.101463323_101463328delinsATTTTT	NCBI36
NG_008986.1:g.24086_24091delinsAAAAAT , LRG_406:g.24086_24091delinsAAAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*1006_*1011delinsAAAAAT (COX15) MANE Select	ENSP00000016171.6:n.*1006_*1011delinsAAAAAT
ENST00000649102.1:c.*460+2767_*460+2772delinsAAAAAT	ENSP00000497114.1:n.*460+2767_*460+2772delinsAAAAAT
ENST00000016171.5:c.*1006_*1011delinsAAAAAT (COX15)	ENSP00000016171.5:n.*1006_*1011delinsAAAAAT
ENST00000370483.9:c.1102-102_1102-97delinsAAAAAT (COX15)	ENSP00000359514.5:n.1102-102_1102-97delinsAAAAAT
ENST00000493385.5:n.117-9342_117-9337delinsATTTTT (CUTC)
NM_004376.5:c.1102-102_1102-97delinsAAAAAT , LRG_406t2:c.1102-102_1102-97delinsAAAAAT (COX15)	NP_004367.2:n.1102-102_1102-97delinsAAAAAT
NM_078470.4:c.*1006_*1011delinsAAAAAT , LRG_406t1:c.*1006_*1011delinsAAAAAT (COX15)	NP_510870.1:n.*1006_*1011delinsAAAAAT
XM_005269539.3:c.1101+2767_1101+2772delinsAAAAAT (COX15)	XP_005269596.1:n.1101+2767_1101+2772delinsAAAAAT
XM_006717633.2:c.*1187_*1192delinsAAAAAT (COX15)	XP_006717696.1:n.*1187_*1192delinsAAAAAT
XM_006717634.2:c.*49+2767_*49+2772delinsAAAAAT (COX15)	XP_006717697.1:n.*49+2767_*49+2772delinsAAAAAT
XM_011539298.1:c.*50-102_*50-97delinsAAAAAT (COX15)	XP_011537600.1:n.*50-102_*50-97delinsAAAAAT
NM_001320974.1:c.1101+2767_1101+2772delinsAAAAAT (COX15)	NP_001307903.1:n.1101+2767_1101+2772delinsAAAAAT
NM_001320975.1:c.*1187_*1192delinsAAAAAT (COX15)	NP_001307904.1:n.*1187_*1192delinsAAAAAT
NM_001320976.1:c.*1006_*1011delinsAAAAAT (COX15)	NP_001307905.1:n.*1006_*1011delinsAAAAAT
NM_004376.6:c.1102-102_1102-97delinsAAAAAT (COX15)	NP_004367.2:n.1102-102_1102-97delinsAAAAAT
NM_078470.5:c.*1006_*1011delinsAAAAAT (COX15)	NP_510870.1:n.*1006_*1011delinsAAAAAT
XM_006717634.3:c.*49+2767_*49+2772delinsAAAAAT (COX15)	XP_006717697.1:n.*49+2767_*49+2772delinsAAAAAT
XM_011539298.2:c.*50-102_*50-97delinsAAAAAT (COX15)	XP_011537600.1:n.*50-102_*50-97delinsAAAAAT
NM_001320974.2:c.1101+2767_1101+2772delinsAAAAAT (COX15)	NP_001307903.1:n.1101+2767_1101+2772delinsAAAAAT
NM_001320975.2:c.*1187_*1192delinsAAAAAT (COX15)	NP_001307904.1:n.*1187_*1192delinsAAAAAT
NM_001320976.2:c.*1006_*1011delinsAAAAAT (COX15)	NP_001307905.1:n.*1006_*1011delinsAAAAAT
NM_001372024.1:c.*225_*230delinsAAAAAT (COX15)	NP_001358953.1:n.*225_*230delinsAAAAAT
NM_001372025.1:c.*1006_*1011delinsAAAAAT (COX15)	NP_001358954.1:n.*1006_*1011delinsAAAAAT
NM_001372026.1:c.*1006_*1011delinsAAAAAT (COX15)	NP_001358955.1:n.*1006_*1011delinsAAAAAT
NM_001372027.1:c.*1110_*1115delinsAAAAAT (COX15)	NP_001358956.1:n.*1110_*1115delinsAAAAAT
NM_001372028.1:c.*433_*438delinsAAAAAT (COX15)	NP_001358957.1:n.*433_*438delinsAAAAAT
NM_004376.7:c.1102-102_1102-97delinsAAAAAT (COX15)	NP_004367.2:n.1102-102_1102-97delinsAAAAAT
NM_078470.6:c.*1006_*1011delinsAAAAAT (COX15) MANE Select	NP_510870.1:n.*1006_*1011delinsAAAAAT
NR_164009.1:n.2079_2084delinsAAAAAT (COX15)