Canonical Allele Identifier: CA670625461

Gene: COX15 CUTC

Linked Data

• dbSNP Id: rs1206052083
• MyVariant Identifiers: chr10:g.101473239_101473243del (hg19) ; chr10:g.99713482_99713486del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713484_99713488del , CM000672.2:g.99713484_99713488del	GRCh38
NC_000010.10:g.101473241_101473245del , CM000672.1:g.101473241_101473245del	GRCh37
NC_000010.9:g.101463231_101463235del	NCBI36
NG_008986.1:g.24181_24185del , LRG_406:g.24181_24185del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*1101_*1105del (COX15) MANE Select	ENSP00000016171.6:n.*1101_*1105del
ENST00000649102.1:c.*460+2862_*460+2866del	ENSP00000497114.1:n.*460+2862_*460+2866del
ENST00000370483.9:c.1102-7_1102-3del (COX15)	ENSP00000359514.5:n.1102-7_1102-3del
ENST00000493385.5:n.117-9434_117-9430del (CUTC)
NM_004376.5:c.1102-7_1102-3del , LRG_406t2:c.1102-7_1102-3del (COX15)	NP_004367.2:n.1102-7_1102-3del
NM_078470.4:c.*1101_*1105del , LRG_406t1:c.*1101_*1105del (COX15)	NP_510870.1:n.*1101_*1105del
XM_005269539.3:c.1101+2862_1101+2866del (COX15)	XP_005269596.1:n.1101+2862_1101+2866del
XM_006717633.2:c.*1282_*1286del (COX15)	XP_006717696.1:n.*1282_*1286del
XM_006717634.2:c.*49+2862_*49+2866del (COX15)	XP_006717697.1:n.*49+2862_*49+2866del
XM_011539298.1:c.*50-7_*50-3del (COX15)	XP_011537600.1:n.*50-7_*50-3del
NM_001320974.1:c.1101+2862_1101+2866del (COX15)	NP_001307903.1:n.1101+2862_1101+2866del
NM_001320975.1:c.*1282_*1286del (COX15)	NP_001307904.1:n.*1282_*1286del
NM_001320976.1:c.*1101_*1105del (COX15)	NP_001307905.1:n.*1101_*1105del
NM_004376.6:c.1102-7_1102-3del (COX15)	NP_004367.2:n.1102-7_1102-3del
NM_078470.5:c.*1101_*1105del (COX15)	NP_510870.1:n.*1101_*1105del
XM_006717634.3:c.*49+2862_*49+2866del (COX15)	XP_006717697.1:n.*49+2862_*49+2866del
XM_011539298.2:c.*50-7_*50-3del (COX15)	XP_011537600.1:n.*50-7_*50-3del
NM_001320974.2:c.1101+2862_1101+2866del (COX15)	NP_001307903.1:n.1101+2862_1101+2866del
NM_001320975.2:c.*1282_*1286del (COX15)	NP_001307904.1:n.*1282_*1286del
NM_001320976.2:c.*1101_*1105del (COX15)	NP_001307905.1:n.*1101_*1105del
NM_001372024.1:c.*320_*324del (COX15)	NP_001358953.1:n.*320_*324del
NM_001372025.1:c.*1101_*1105del (COX15)	NP_001358954.1:n.*1101_*1105del
NM_001372026.1:c.*1101_*1105del (COX15)	NP_001358955.1:n.*1101_*1105del
NM_001372027.1:c.*1205_*1209del (COX15)	NP_001358956.1:n.*1205_*1209del
NM_001372028.1:c.*528_*532del (COX15)	NP_001358957.1:n.*528_*532del
NM_004376.7:c.1102-7_1102-3del (COX15)	NP_004367.2:n.1102-7_1102-3del
NM_078470.6:c.*1101_*1105del (COX15) MANE Select	NP_510870.1:n.*1101_*1105del
NR_164009.1:n.2174_2178del (COX15)