Canonical Allele Identifier: CA1931452037

Linked Data

dbSNP Id: rs2036459148

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99713328del , CM000672.2:g.99713328del GRCh38
NC_000010.10:g.101473085del , CM000672.1:g.101473085del GRCh37
NC_000010.9:g.101463075del NCBI36
NG_008986.1:g.24341del , LRG_406:g.24341del

Transcript Alleles

HGVS Amino-acid Change
ENST00000016171.6:c.*1261del (COX15) MANE Select ENSP00000016171.6:n.*1261del
ENST00000649102.1:c.*460+3022del ENSP00000497114.1:n.*460+3022del
ENST00000370483.9:c.*88del (COX15) ENSP00000359514.5:n.*88del
ENST00000493385.5:n.117-9590del (CUTC)
NM_004376.5:c.*88del , LRG_406t2:c.*88del (COX15) NP_004367.2:n.*88del
NM_078470.4:c.*1261del , LRG_406t1:c.*1261del (COX15) NP_510870.1:n.*1261del
XM_005269539.3:c.1101+3022del (COX15) XP_005269596.1:n.1101+3022del
XM_006717633.2:c.*1442del (COX15) XP_006717696.1:n.*1442del
XM_006717634.2:c.*49+3022del (COX15) XP_006717697.1:n.*49+3022del
NM_001320974.1:c.1101+3022del (COX15) NP_001307903.1:n.1101+3022del
NM_001320975.1:c.*1442del (COX15) NP_001307904.1:n.*1442del
NM_001320976.1:c.*1261del (COX15) NP_001307905.1:n.*1261del
NM_004376.6:c.*88del (COX15) NP_004367.2:n.*88del
NM_078470.5:c.*1261del (COX15) NP_510870.1:n.*1261del
XM_006717634.3:c.*49+3022del (COX15) XP_006717697.1:n.*49+3022del
XM_011539298.2:c.*203del (COX15) XP_011537600.1:n.*203del
NM_001320974.2:c.1101+3022del (COX15) NP_001307903.1:n.1101+3022del
NM_001320975.2:c.*1442del (COX15) NP_001307904.1:n.*1442del
NM_001320976.2:c.*1261del (COX15) NP_001307905.1:n.*1261del
NM_001372024.1:c.*480del (COX15) NP_001358953.1:n.*480del
NM_001372025.1:c.*1261del (COX15) NP_001358954.1:n.*1261del
NM_001372026.1:c.*1261del (COX15) NP_001358955.1:n.*1261del
NM_001372027.1:c.*1365del (COX15) NP_001358956.1:n.*1365del
NM_001372028.1:c.*688del (COX15) NP_001358957.1:n.*688del
NM_004376.7:c.*88del (COX15) NP_004367.2:n.*88del
NM_078470.6:c.*1261del (COX15) MANE Select NP_510870.1:n.*1261del
NR_164009.1:n.2334del (COX15)