Canonical Allele Identifier: CA2574637703

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99727201del , CM000672.2:g.99727201del GRCh38
NC_000010.10:g.101486958del , CM000672.1:g.101486958del GRCh37
NC_000010.9:g.101476948del NCBI36
NG_008986.1:g.10466del , LRG_406:g.10466del

Transcript Alleles

HGVS Amino-acid Change
ENST00000016171.6:c.396-47del (COX15) MANE Select ENSP00000016171.6:n.396-47del
ENST00000649102.1:c.396-130del ENSP00000497114.1:n.396-130del
ENST00000016171.5:c.396-47del (COX15) ENSP00000016171.5:n.396-47del
ENST00000370483.9:c.396-47del (COX15) ENSP00000359514.5:n.396-47del
ENST00000493385.5:n.309+4091del (CUTC)
NM_004376.5:c.396-47del , LRG_406t2:c.396-47del (COX15) NP_004367.2:n.396-47del
NM_078470.4:c.396-47del , LRG_406t1:c.396-47del (COX15) NP_510870.1:n.396-47del
XM_005269539.3:c.396-47del (COX15) XP_005269596.1:n.396-47del
XM_006717633.2:c.396-47del (COX15) XP_006717696.1:n.396-47del
XM_006717634.2:c.396-47del (COX15) XP_006717697.1:n.396-47del
XM_011539298.1:c.396-47del (COX15) XP_011537600.1:n.396-47del
NM_001320974.1:c.396-47del (COX15) NP_001307903.1:n.396-47del
NM_001320975.1:c.396-47del (COX15) NP_001307904.1:n.396-47del
NM_001320976.1:c.-59-130del (COX15) NP_001307905.1:n.-59-130del
NM_004376.6:c.396-47del (COX15) NP_004367.2:n.396-47del
NM_078470.5:c.396-47del (COX15) NP_510870.1:n.396-47del
XM_006717634.3:c.396-47del (COX15) XP_006717697.1:n.396-47del
XM_011539298.2:c.396-47del (COX15) XP_011537600.1:n.396-47del
NM_001320974.2:c.396-47del (COX15) NP_001307903.1:n.396-47del
NM_001320975.2:c.396-47del (COX15) NP_001307904.1:n.396-47del
NM_001320976.2:c.-59-130del (COX15) NP_001307905.1:n.-59-130del
NM_001372024.1:c.396-47del (COX15) NP_001358953.1:n.396-47del
NM_001372025.1:c.396-47del (COX15) NP_001358954.1:n.396-47del
NM_001372026.1:c.396-47del (COX15) NP_001358955.1:n.396-47del
NM_001372027.1:c.396-47del (COX15) NP_001358956.1:n.396-47del
NM_001372028.1:c.396-47del (COX15) NP_001358957.1:n.396-47del
NM_004376.7:c.396-47del (COX15) NP_004367.2:n.396-47del
NM_078470.6:c.396-47del (COX15) MANE Select NP_510870.1:n.396-47del
NR_164009.1:n.474-130del (COX15)