Canonical Allele Identifier: CA931706120

Linked Data

dbSNP Id: rs2036458949

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99713318_99713319del , CM000672.2:g.99713318_99713319del GRCh38
NC_000010.10:g.101473075_101473076del , CM000672.1:g.101473075_101473076del GRCh37
NC_000010.9:g.101463065_101463066del NCBI36
NG_008986.1:g.24349_24350del , LRG_406:g.24349_24350del

Transcript Alleles

HGVS Amino-acid Change
ENST00000016171.6:c.*1269_*1270del (COX15) MANE Select ENSP00000016171.6:n.*1269_*1270del
ENST00000649102.1:c.*460+3030_*460+3031del ENSP00000497114.1:n.*460+3030_*460+3031del
ENST00000370483.9:c.*96_*97del (COX15) ENSP00000359514.5:n.*96_*97del
ENST00000493385.5:n.117-9600_117-9599del (CUTC)
NM_004376.5:c.*96_*97del , LRG_406t2:c.*96_*97del (COX15) NP_004367.2:n.*96_*97del
NM_078470.4:c.*1269_*1270del , LRG_406t1:c.*1269_*1270del (COX15) NP_510870.1:n.*1269_*1270del
XM_005269539.3:c.1101+3030_1101+3031del (COX15) XP_005269596.1:n.1101+3030_1101+3031del
XM_006717633.2:c.*1450_*1451del (COX15) XP_006717696.1:n.*1450_*1451del
XM_006717634.2:c.*49+3030_*49+3031del (COX15) XP_006717697.1:n.*49+3030_*49+3031del
NM_001320974.1:c.1101+3030_1101+3031del (COX15) NP_001307903.1:n.1101+3030_1101+3031del
NM_001320975.1:c.*1450_*1451del (COX15) NP_001307904.1:n.*1450_*1451del
NM_001320976.1:c.*1269_*1270del (COX15) NP_001307905.1:n.*1269_*1270del
NM_004376.6:c.*96_*97del (COX15) NP_004367.2:n.*96_*97del
NM_078470.5:c.*1269_*1270del (COX15) NP_510870.1:n.*1269_*1270del
XM_006717634.3:c.*49+3030_*49+3031del (COX15) XP_006717697.1:n.*49+3030_*49+3031del
XM_011539298.2:c.*211_*212del (COX15) XP_011537600.1:n.*211_*212del
NM_001320974.2:c.1101+3030_1101+3031del (COX15) NP_001307903.1:n.1101+3030_1101+3031del
NM_001320975.2:c.*1450_*1451del (COX15) NP_001307904.1:n.*1450_*1451del
NM_001320976.2:c.*1269_*1270del (COX15) NP_001307905.1:n.*1269_*1270del
NM_001372024.1:c.*488_*489del (COX15) NP_001358953.1:n.*488_*489del
NM_001372025.1:c.*1269_*1270del (COX15) NP_001358954.1:n.*1269_*1270del
NM_001372026.1:c.*1269_*1270del (COX15) NP_001358955.1:n.*1269_*1270del
NM_001372027.1:c.*1373_*1374del (COX15) NP_001358956.1:n.*1373_*1374del
NM_001372028.1:c.*696_*697del (COX15) NP_001358957.1:n.*696_*697del
NM_004376.7:c.*96_*97del (COX15) NP_004367.2:n.*96_*97del
NM_078470.6:c.*1269_*1270del (COX15) MANE Select NP_510870.1:n.*1269_*1270del
NR_164009.1:n.2342_2343del (COX15)