Canonical Allele Identifier: CA378101262

Linked Data

dbSNP Id: rs2036508081

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99714621C>T , CM000672.2:g.99714621C>T GRCh38
NC_000010.10:g.101474378C>T , CM000672.1:g.101474378C>T GRCh37
NC_000010.9:g.101464368C>T NCBI36
NG_008986.1:g.23046G>A , LRG_406:g.23046G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000016171.6:c.1199G>A (COX15) MANE Select ENSP00000016171.6:p.Trp400Ter
ENST00000649102.1:c.*460+1727G>A ENSP00000497114.1:n.*460+1727G>A
ENST00000016171.5:c.1199G>A (COX15) ENSP00000016171.5:p.Trp400Ter
ENST00000370483.9:c.1102-1142G>A (COX15) ENSP00000359514.5:n.1102-1142G>A
ENST00000493385.5:n.117-8297C>T (CUTC)
NM_004376.5:c.1102-1142G>A , LRG_406t2:c.1102-1142G>A (COX15) NP_004367.2:n.1102-1142G>A
NM_078470.4:c.1199G>A , LRG_406t1:c.1199G>A (COX15) NP_510870.1:p.Trp400Ter
XM_005269539.3:c.1101+1727G>A (COX15) XP_005269596.1:n.1101+1727G>A
XM_006717633.2:c.*147G>A (COX15) XP_006717696.1:n.*147G>A
XM_006717634.2:c.*49+1727G>A (COX15) XP_006717697.1:n.*49+1727G>A
XM_011539298.1:c.*50-1142G>A (COX15) XP_011537600.1:n.*50-1142G>A
NM_001320974.1:c.1101+1727G>A (COX15) NP_001307903.1:n.1101+1727G>A
NM_001320975.1:c.*147G>A (COX15) NP_001307904.1:n.*147G>A
NM_001320976.1:c.662G>A (COX15) NP_001307905.1:p.Trp221Ter
NM_004376.6:c.1102-1142G>A (COX15) NP_004367.2:n.1102-1142G>A
NM_078470.5:c.1199G>A (COX15) NP_510870.1:p.Trp400Ter
XM_006717634.3:c.*49+1727G>A (COX15) XP_006717697.1:n.*49+1727G>A
XM_011539298.2:c.*50-1142G>A (COX15) XP_011537600.1:n.*50-1142G>A
NM_001320974.2:c.1101+1727G>A (COX15) NP_001307903.1:n.1101+1727G>A
NM_001320975.2:c.*147G>A (COX15) NP_001307904.1:n.*147G>A
NM_001320976.2:c.662G>A (COX15) NP_001307905.1:p.Trp221Ter
NM_001372024.1:c.1102-657G>A (COX15) NP_001358953.1:n.1102-657G>A
NM_001372025.1:c.1217G>A (COX15) NP_001358954.1:p.Trp406Ter
NM_001372026.1:c.1172G>A (COX15) NP_001358955.1:p.Trp391Ter
NM_001372027.1:c.*70G>A (COX15) NP_001358956.1:n.*70G>A
NM_001372028.1:c.*50-657G>A (COX15) NP_001358957.1:n.*50-657G>A
NM_004376.7:c.1102-1142G>A (COX15) NP_004367.2:n.1102-1142G>A
NM_078470.6:c.1199G>A (COX15) MANE Select NP_510870.1:p.Trp400Ter
NR_164009.1:n.1039G>A (COX15)