Canonical Allele Identifier: CA2610488839

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99713405_99713408dup , CM000672.2:g.99713405_99713408dup GRCh38
NC_000010.10:g.101473162_101473165dup , CM000672.1:g.101473162_101473165dup GRCh37
NC_000010.9:g.101463152_101463155dup NCBI36
NG_008986.1:g.24262_24265dup , LRG_406:g.24262_24265dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000016171.6:c.*1182_*1185dup (COX15) MANE Select ENSP00000016171.6:n.*1182_*1185dup
ENST00000649102.1:c.*460+2943_*460+2946dup ENSP00000497114.1:n.*460+2943_*460+2946dup
ENST00000370483.9:c.*9_*12dup (COX15) ENSP00000359514.5:n.*9_*12dup
ENST00000493385.5:n.117-9513_117-9510dup (CUTC)
NM_004376.5:c.*9_*12dup , LRG_406t2:c.*9_*12dup (COX15) NP_004367.2:n.*9_*12dup
NM_078470.4:c.*1182_*1185dup , LRG_406t1:c.*1182_*1185dup (COX15) NP_510870.1:n.*1182_*1185dup
XM_005269539.3:c.1101+2943_1101+2946dup (COX15) XP_005269596.1:n.1101+2943_1101+2946dup
XM_006717633.2:c.*1363_*1366dup (COX15) XP_006717696.1:n.*1363_*1366dup
XM_006717634.2:c.*49+2943_*49+2946dup (COX15) XP_006717697.1:n.*49+2943_*49+2946dup
XM_011539298.1:c.*124_*127dup (COX15) XP_011537600.1:n.*124_*127dup
NM_001320974.1:c.1101+2943_1101+2946dup (COX15) NP_001307903.1:n.1101+2943_1101+2946dup
NM_001320975.1:c.*1363_*1366dup (COX15) NP_001307904.1:n.*1363_*1366dup
NM_001320976.1:c.*1182_*1185dup (COX15) NP_001307905.1:n.*1182_*1185dup
NM_004376.6:c.*9_*12dup (COX15) NP_004367.2:n.*9_*12dup
NM_078470.5:c.*1182_*1185dup (COX15) NP_510870.1:n.*1182_*1185dup
XM_006717634.3:c.*49+2943_*49+2946dup (COX15) XP_006717697.1:n.*49+2943_*49+2946dup
XM_011539298.2:c.*124_*127dup (COX15) XP_011537600.1:n.*124_*127dup
NM_001320974.2:c.1101+2943_1101+2946dup (COX15) NP_001307903.1:n.1101+2943_1101+2946dup
NM_001320975.2:c.*1363_*1366dup (COX15) NP_001307904.1:n.*1363_*1366dup
NM_001320976.2:c.*1182_*1185dup (COX15) NP_001307905.1:n.*1182_*1185dup
NM_001372024.1:c.*401_*404dup (COX15) NP_001358953.1:n.*401_*404dup
NM_001372025.1:c.*1182_*1185dup (COX15) NP_001358954.1:n.*1182_*1185dup
NM_001372026.1:c.*1182_*1185dup (COX15) NP_001358955.1:n.*1182_*1185dup
NM_001372027.1:c.*1286_*1289dup (COX15) NP_001358956.1:n.*1286_*1289dup
NM_001372028.1:c.*609_*612dup (COX15) NP_001358957.1:n.*609_*612dup
NM_004376.7:c.*9_*12dup (COX15) NP_004367.2:n.*9_*12dup
NM_078470.6:c.*1182_*1185dup (COX15) MANE Select NP_510870.1:n.*1182_*1185dup
NR_164009.1:n.2255_2258dup (COX15)