Canonical Allele Identifier: CA653854543

Gene: COX15 CUTC

Linked Data

• COSMIC: COSN17182226 ; COSN20056491

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713307_99713308insG , CM000672.2:g.99713307_99713308insG	GRCh38
NC_000010.10:g.101473064_101473065insG , CM000672.1:g.101473064_101473065insG	GRCh37
NC_000010.9:g.101463054_101463055insG	NCBI36
NG_008986.1:g.24359_24360insC , LRG_406:g.24359_24360insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*1279_*1280insC (COX15) MANE Select	ENSP00000016171.6:n.*1279_*1280insC
ENST00000649102.1:c.*460+3040_*460+3041insC	ENSP00000497114.1:n.*460+3040_*460+3041insC
ENST00000370483.9:c.*106_*107insC (COX15)	ENSP00000359514.5:n.*106_*107insC
ENST00000493385.5:n.117-9611_117-9610insG (CUTC)
NM_004376.5:c.*106_*107insC , LRG_406t2:c.*106_*107insC (COX15)	NP_004367.2:n.*106_*107insC
NM_078470.4:c.*1279_*1280insC , LRG_406t1:c.*1279_*1280insC (COX15)	NP_510870.1:n.*1279_*1280insC
XM_005269539.3:c.1101+3040_1101+3041insC (COX15)	XP_005269596.1:n.1101+3040_1101+3041insC
XM_006717633.2:c.*1460_*1461insC (COX15)	XP_006717696.1:n.*1460_*1461insC
XM_006717634.2:c.*49+3040_*49+3041insC (COX15)	XP_006717697.1:n.*49+3040_*49+3041insC
NM_001320974.1:c.1101+3040_1101+3041insC (COX15)	NP_001307903.1:n.1101+3040_1101+3041insC
NM_001320975.1:c.*1460_*1461insC (COX15)	NP_001307904.1:n.*1460_*1461insC
NM_001320976.1:c.*1279_*1280insC (COX15)	NP_001307905.1:n.*1279_*1280insC
NM_004376.6:c.*106_*107insC (COX15)	NP_004367.2:n.*106_*107insC
NM_078470.5:c.*1279_*1280insC (COX15)	NP_510870.1:n.*1279_*1280insC
XM_006717634.3:c.*49+3040_*49+3041insC (COX15)	XP_006717697.1:n.*49+3040_*49+3041insC
XM_011539298.2:c.*221_*222insC (COX15)	XP_011537600.1:n.*221_*222insC
NM_001320974.2:c.1101+3040_1101+3041insC (COX15)	NP_001307903.1:n.1101+3040_1101+3041insC
NM_001320975.2:c.*1460_*1461insC (COX15)	NP_001307904.1:n.*1460_*1461insC
NM_001320976.2:c.*1279_*1280insC (COX15)	NP_001307905.1:n.*1279_*1280insC
NM_001372024.1:c.*498_*499insC (COX15)	NP_001358953.1:n.*498_*499insC
NM_001372025.1:c.*1279_*1280insC (COX15)	NP_001358954.1:n.*1279_*1280insC
NM_001372026.1:c.*1279_*1280insC (COX15)	NP_001358955.1:n.*1279_*1280insC
NM_001372027.1:c.*1383_*1384insC (COX15)	NP_001358956.1:n.*1383_*1384insC
NM_001372028.1:c.*706_*707insC (COX15)	NP_001358957.1:n.*706_*707insC
NM_004376.7:c.*106_*107insC (COX15)	NP_004367.2:n.*106_*107insC
NM_078470.6:c.*1279_*1280insC (COX15) MANE Select	NP_510870.1:n.*1279_*1280insC
NR_164009.1:n.2352_2353insC (COX15)