Canonical Allele Identifier: CA2610489299

Gene: COX15 CUTC

Linked Data

• gnomAD v4: 10-99713801-C-CCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713801_99713802insCTG , CM000672.2:g.99713801_99713802insCTG	GRCh38
NC_000010.10:g.101473558_101473559insCTG , CM000672.1:g.101473558_101473559insCTG	GRCh37
NC_000010.9:g.101463548_101463549insCTG	NCBI36
NG_008986.1:g.23865_23866insCAG , LRG_406:g.23865_23866insCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*785_*786insCAG (COX15) MANE Select	ENSP00000016171.6:n.*785_*786insCAG
ENST00000649102.1:c.*460+2546_*460+2547insCAG	ENSP00000497114.1:n.*460+2546_*460+2547insCAG
ENST00000016171.5:c.*785_*786insCAG (COX15)	ENSP00000016171.5:n.*785_*786insCAG
ENST00000370483.9:c.1102-323_1102-322insCAG (COX15)	ENSP00000359514.5:n.1102-323_1102-322insCAG
ENST00000493385.5:n.117-9117_117-9116insCTG (CUTC)
NM_004376.5:c.1102-323_1102-322insCAG , LRG_406t2:c.1102-323_1102-322insCAG (COX15)	NP_004367.2:n.1102-323_1102-322insCAG
NM_078470.4:c.*785_*786insCAG , LRG_406t1:c.*785_*786insCAG (COX15)	NP_510870.1:n.*785_*786insCAG
XM_005269539.3:c.1101+2546_1101+2547insCAG (COX15)	XP_005269596.1:n.1101+2546_1101+2547insCAG
XM_006717633.2:c.*966_*967insCAG (COX15)	XP_006717696.1:n.*966_*967insCAG
XM_006717634.2:c.*49+2546_*49+2547insCAG (COX15)	XP_006717697.1:n.*49+2546_*49+2547insCAG
XM_011539298.1:c.*50-323_*50-322insCAG (COX15)	XP_011537600.1:n.*50-323_*50-322insCAG
NM_001320974.1:c.1101+2546_1101+2547insCAG (COX15)	NP_001307903.1:n.1101+2546_1101+2547insCAG
NM_001320975.1:c.*966_*967insCAG (COX15)	NP_001307904.1:n.*966_*967insCAG
NM_001320976.1:c.*785_*786insCAG (COX15)	NP_001307905.1:n.*785_*786insCAG
NM_004376.6:c.1102-323_1102-322insCAG (COX15)	NP_004367.2:n.1102-323_1102-322insCAG
NM_078470.5:c.*785_*786insCAG (COX15)	NP_510870.1:n.*785_*786insCAG
XM_006717634.3:c.*49+2546_*49+2547insCAG (COX15)	XP_006717697.1:n.*49+2546_*49+2547insCAG
XM_011539298.2:c.*50-323_*50-322insCAG (COX15)	XP_011537600.1:n.*50-323_*50-322insCAG
NM_001320974.2:c.1101+2546_1101+2547insCAG (COX15)	NP_001307903.1:n.1101+2546_1101+2547insCAG
NM_001320975.2:c.*966_*967insCAG (COX15)	NP_001307904.1:n.*966_*967insCAG
NM_001320976.2:c.*785_*786insCAG (COX15)	NP_001307905.1:n.*785_*786insCAG
NM_001372024.1:c.*4_*5insCAG (COX15)	NP_001358953.1:n.*4_*5insCAG
NM_001372025.1:c.*785_*786insCAG (COX15)	NP_001358954.1:n.*785_*786insCAG
NM_001372026.1:c.*785_*786insCAG (COX15)	NP_001358955.1:n.*785_*786insCAG
NM_001372027.1:c.*889_*890insCAG (COX15)	NP_001358956.1:n.*889_*890insCAG
NM_001372028.1:c.*212_*213insCAG (COX15)	NP_001358957.1:n.*212_*213insCAG
NM_004376.7:c.1102-323_1102-322insCAG (COX15)	NP_004367.2:n.1102-323_1102-322insCAG
NM_078470.6:c.*785_*786insCAG (COX15) MANE Select	NP_510870.1:n.*785_*786insCAG
NR_164009.1:n.1858_1859insCAG (COX15)