Canonical Allele Identifier: CA1931452030

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713316_99713318delinsATC , CM000672.2:g.99713316_99713318delinsATC	GRCh38
NC_000010.10:g.101473073_101473075delinsATC , CM000672.1:g.101473073_101473075delinsATC	GRCh37
NC_000010.9:g.101463063_101463065delinsATC	NCBI36
NG_008986.1:g.24349_24351delinsGAT , LRG_406:g.24349_24351delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*1269_*1271delinsGAT (COX15) MANE Select	ENSP00000016171.6:n.*1269_*1271delinsGAT
ENST00000649102.1:c.*460+3030_*460+3032delinsGAT	ENSP00000497114.1:n.*460+3030_*460+3032delinsGAT
ENST00000370483.9:c.*96_*98delinsGAT (COX15)	ENSP00000359514.5:n.*96_*98delinsGAT
ENST00000493385.5:n.117-9602_117-9600delinsATC (CUTC)
NM_004376.5:c.*96_*98delinsGAT , LRG_406t2:c.*96_*98delinsGAT (COX15)	NP_004367.2:n.*96_*98delinsGAT
NM_078470.4:c.*1269_*1271delinsGAT , LRG_406t1:c.*1269_*1271delinsGAT (COX15)	NP_510870.1:n.*1269_*1271delinsGAT
XM_005269539.3:c.1101+3030_1101+3032delinsGAT (COX15)	XP_005269596.1:n.1101+3030_1101+3032delinsGAT
XM_006717633.2:c.*1450_*1452delinsGAT (COX15)	XP_006717696.1:n.*1450_*1452delinsGAT
XM_006717634.2:c.*49+3030_*49+3032delinsGAT (COX15)	XP_006717697.1:n.*49+3030_*49+3032delinsGAT
NM_001320974.1:c.1101+3030_1101+3032delinsGAT (COX15)	NP_001307903.1:n.1101+3030_1101+3032delinsGAT
NM_001320975.1:c.*1450_*1452delinsGAT (COX15)	NP_001307904.1:n.*1450_*1452delinsGAT
NM_001320976.1:c.*1269_*1271delinsGAT (COX15)	NP_001307905.1:n.*1269_*1271delinsGAT
NM_004376.6:c.*96_*98delinsGAT (COX15)	NP_004367.2:n.*96_*98delinsGAT
NM_078470.5:c.*1269_*1271delinsGAT (COX15)	NP_510870.1:n.*1269_*1271delinsGAT
XM_006717634.3:c.*49+3030_*49+3032delinsGAT (COX15)	XP_006717697.1:n.*49+3030_*49+3032delinsGAT
XM_011539298.2:c.*211_*213delinsGAT (COX15)	XP_011537600.1:n.*211_*213delinsGAT
NM_001320974.2:c.1101+3030_1101+3032delinsGAT (COX15)	NP_001307903.1:n.1101+3030_1101+3032delinsGAT
NM_001320975.2:c.*1450_*1452delinsGAT (COX15)	NP_001307904.1:n.*1450_*1452delinsGAT
NM_001320976.2:c.*1269_*1271delinsGAT (COX15)	NP_001307905.1:n.*1269_*1271delinsGAT
NM_001372024.1:c.*488_*490delinsGAT (COX15)	NP_001358953.1:n.*488_*490delinsGAT
NM_001372025.1:c.*1269_*1271delinsGAT (COX15)	NP_001358954.1:n.*1269_*1271delinsGAT
NM_001372026.1:c.*1269_*1271delinsGAT (COX15)	NP_001358955.1:n.*1269_*1271delinsGAT
NM_001372027.1:c.*1373_*1375delinsGAT (COX15)	NP_001358956.1:n.*1373_*1375delinsGAT
NM_001372028.1:c.*696_*698delinsGAT (COX15)	NP_001358957.1:n.*696_*698delinsGAT
NM_004376.7:c.*96_*98delinsGAT (COX15)	NP_004367.2:n.*96_*98delinsGAT
NM_078470.6:c.*1269_*1271delinsGAT (COX15) MANE Select	NP_510870.1:n.*1269_*1271delinsGAT
NR_164009.1:n.2342_2344delinsGAT (COX15)