Canonical Allele Identifier: CA2610488838

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99713400_99713409dup , CM000672.2:g.99713400_99713409dup GRCh38
NC_000010.10:g.101473157_101473166dup , CM000672.1:g.101473157_101473166dup GRCh37
NC_000010.9:g.101463147_101463156dup NCBI36
NG_008986.1:g.24259_24268dup , LRG_406:g.24259_24268dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000016171.6:c.*1179_*1188dup (COX15) MANE Select ENSP00000016171.6:n.*1179_*1188dup
ENST00000649102.1:c.*460+2940_*460+2949dup ENSP00000497114.1:n.*460+2940_*460+2949dup
ENST00000370483.9:c.*6_*15dup (COX15) ENSP00000359514.5:n.*6_*15dup
ENST00000493385.5:n.117-9518_117-9509dup (CUTC)
NM_004376.5:c.*6_*15dup , LRG_406t2:c.*6_*15dup (COX15) NP_004367.2:n.*6_*15dup
NM_078470.4:c.*1179_*1188dup , LRG_406t1:c.*1179_*1188dup (COX15) NP_510870.1:n.*1179_*1188dup
XM_005269539.3:c.1101+2940_1101+2949dup (COX15) XP_005269596.1:n.1101+2940_1101+2949dup
XM_006717633.2:c.*1360_*1369dup (COX15) XP_006717696.1:n.*1360_*1369dup
XM_006717634.2:c.*49+2940_*49+2949dup (COX15) XP_006717697.1:n.*49+2940_*49+2949dup
XM_011539298.1:c.*121_*130dup (COX15) XP_011537600.1:n.*121_*130dup
NM_001320974.1:c.1101+2940_1101+2949dup (COX15) NP_001307903.1:n.1101+2940_1101+2949dup
NM_001320975.1:c.*1360_*1369dup (COX15) NP_001307904.1:n.*1360_*1369dup
NM_001320976.1:c.*1179_*1188dup (COX15) NP_001307905.1:n.*1179_*1188dup
NM_004376.6:c.*6_*15dup (COX15) NP_004367.2:n.*6_*15dup
NM_078470.5:c.*1179_*1188dup (COX15) NP_510870.1:n.*1179_*1188dup
XM_006717634.3:c.*49+2940_*49+2949dup (COX15) XP_006717697.1:n.*49+2940_*49+2949dup
XM_011539298.2:c.*121_*130dup (COX15) XP_011537600.1:n.*121_*130dup
NM_001320974.2:c.1101+2940_1101+2949dup (COX15) NP_001307903.1:n.1101+2940_1101+2949dup
NM_001320975.2:c.*1360_*1369dup (COX15) NP_001307904.1:n.*1360_*1369dup
NM_001320976.2:c.*1179_*1188dup (COX15) NP_001307905.1:n.*1179_*1188dup
NM_001372024.1:c.*398_*407dup (COX15) NP_001358953.1:n.*398_*407dup
NM_001372025.1:c.*1179_*1188dup (COX15) NP_001358954.1:n.*1179_*1188dup
NM_001372026.1:c.*1179_*1188dup (COX15) NP_001358955.1:n.*1179_*1188dup
NM_001372027.1:c.*1283_*1292dup (COX15) NP_001358956.1:n.*1283_*1292dup
NM_001372028.1:c.*606_*615dup (COX15) NP_001358957.1:n.*606_*615dup
NM_004376.7:c.*6_*15dup (COX15) NP_004367.2:n.*6_*15dup
NM_078470.6:c.*1179_*1188dup (COX15) MANE Select NP_510870.1:n.*1179_*1188dup
NR_164009.1:n.2252_2261dup (COX15)