Canonical Allele Identifier: CA931706308

Gene: COX15 CUTC

Linked Data

• gnomAD v3: 10-99713778-C-CCAGCCT
• gnomAD v4: 10-99713778-C-CCAGCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713778_99713779insCAGCCT , CM000672.2:g.99713778_99713779insCAGCCT	GRCh38
NC_000010.10:g.101473535_101473536insCAGCCT , CM000672.1:g.101473535_101473536insCAGCCT	GRCh37
NC_000010.9:g.101463525_101463526insCAGCCT	NCBI36
NG_008986.1:g.23888_23889insAGGCTG , LRG_406:g.23888_23889insAGGCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*808_*809insAGGCTG (COX15) MANE Select	ENSP00000016171.6:n.*808_*809insAGGCTG
ENST00000649102.1:c.*460+2569_*460+2570insAGGCTG	ENSP00000497114.1:n.*460+2569_*460+2570insAGGCTG
ENST00000016171.5:c.*808_*809insAGGCTG (COX15)	ENSP00000016171.5:n.*808_*809insAGGCTG
ENST00000370483.9:c.1102-300_1102-299insAGGCTG (COX15)	ENSP00000359514.5:n.1102-300_1102-299insAGGCTG
ENST00000493385.5:n.117-9140_117-9139insCAGCCT (CUTC)
NM_004376.5:c.1102-300_1102-299insAGGCTG , LRG_406t2:c.1102-300_1102-299insAGGCTG (COX15)	NP_004367.2:n.1102-300_1102-299insAGGCTG
NM_078470.4:c.*808_*809insAGGCTG , LRG_406t1:c.*808_*809insAGGCTG (COX15)	NP_510870.1:n.*808_*809insAGGCTG
XM_005269539.3:c.1101+2569_1101+2570insAGGCTG (COX15)	XP_005269596.1:n.1101+2569_1101+2570insAGGCTG
XM_006717633.2:c.*989_*990insAGGCTG (COX15)	XP_006717696.1:n.*989_*990insAGGCTG
XM_006717634.2:c.*49+2569_*49+2570insAGGCTG (COX15)	XP_006717697.1:n.*49+2569_*49+2570insAGGCTG
XM_011539298.1:c.*50-300_*50-299insAGGCTG (COX15)	XP_011537600.1:n.*50-300_*50-299insAGGCTG
NM_001320974.1:c.1101+2569_1101+2570insAGGCTG (COX15)	NP_001307903.1:n.1101+2569_1101+2570insAGGCTG
NM_001320975.1:c.*989_*990insAGGCTG (COX15)	NP_001307904.1:n.*989_*990insAGGCTG
NM_001320976.1:c.*808_*809insAGGCTG (COX15)	NP_001307905.1:n.*808_*809insAGGCTG
NM_004376.6:c.1102-300_1102-299insAGGCTG (COX15)	NP_004367.2:n.1102-300_1102-299insAGGCTG
NM_078470.5:c.*808_*809insAGGCTG (COX15)	NP_510870.1:n.*808_*809insAGGCTG
XM_006717634.3:c.*49+2569_*49+2570insAGGCTG (COX15)	XP_006717697.1:n.*49+2569_*49+2570insAGGCTG
XM_011539298.2:c.*50-300_*50-299insAGGCTG (COX15)	XP_011537600.1:n.*50-300_*50-299insAGGCTG
NM_001320974.2:c.1101+2569_1101+2570insAGGCTG (COX15)	NP_001307903.1:n.1101+2569_1101+2570insAGGCTG
NM_001320975.2:c.*989_*990insAGGCTG (COX15)	NP_001307904.1:n.*989_*990insAGGCTG
NM_001320976.2:c.*808_*809insAGGCTG (COX15)	NP_001307905.1:n.*808_*809insAGGCTG
NM_001372024.1:c.*27_*28insAGGCTG (COX15)	NP_001358953.1:n.*27_*28insAGGCTG
NM_001372025.1:c.*808_*809insAGGCTG (COX15)	NP_001358954.1:n.*808_*809insAGGCTG
NM_001372026.1:c.*808_*809insAGGCTG (COX15)	NP_001358955.1:n.*808_*809insAGGCTG
NM_001372027.1:c.*912_*913insAGGCTG (COX15)	NP_001358956.1:n.*912_*913insAGGCTG
NM_001372028.1:c.*235_*236insAGGCTG (COX15)	NP_001358957.1:n.*235_*236insAGGCTG
NM_004376.7:c.1102-300_1102-299insAGGCTG (COX15)	NP_004367.2:n.1102-300_1102-299insAGGCTG
NM_078470.6:c.*808_*809insAGGCTG (COX15) MANE Select	NP_510870.1:n.*808_*809insAGGCTG
NR_164009.1:n.1881_1882insAGGCTG (COX15)