Canonical Allele Identifier: CA1931452139

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713461A= , CM000672.2:g.99713461A=	GRCh38
NC_000010.10:g.101473218A= , CM000672.1:g.101473218A=	GRCh37
NC_000010.9:g.101463208A=	NCBI36
NG_008986.1:g.24206T= , LRG_406:g.24206T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*1126T= (COX15) MANE Select	ENSP00000016171.6:n.*1126T=
ENST00000649102.1:c.*460+2887T=	ENSP00000497114.1:n.*460+2887T=
ENST00000370483.9:c.1120T= (COX15)	ENSP00000359514.5:p.Phe374=
ENST00000493385.5:n.117-9457A= (CUTC)
NM_004376.5:c.1120T= , LRG_406t2:c.1120T= (COX15)	NP_004367.2:p.Phe374=
NM_078470.4:c.*1126T= , LRG_406t1:c.*1126T= (COX15)	NP_510870.1:n.*1126T=
XM_005269539.3:c.1101+2887T= (COX15)	XP_005269596.1:n.1101+2887T=
XM_006717633.2:c.*1307T= (COX15)	XP_006717696.1:n.*1307T=
XM_006717634.2:c.*49+2887T= (COX15)	XP_006717697.1:n.*49+2887T=
XM_011539298.1:c.*68T= (COX15)	XP_011537600.1:n.*68T=
NM_001320974.1:c.1101+2887T= (COX15)	NP_001307903.1:n.1101+2887T=
NM_001320975.1:c.*1307T= (COX15)	NP_001307904.1:n.*1307T=
NM_001320976.1:c.*1126T= (COX15)	NP_001307905.1:n.*1126T=
NM_004376.6:c.1120T= (COX15)	NP_004367.2:p.Phe374=
NM_078470.5:c.*1126T= (COX15)	NP_510870.1:n.*1126T=
XM_006717634.3:c.*49+2887T= (COX15)	XP_006717697.1:n.*49+2887T=
XM_011539298.2:c.*68T= (COX15)	XP_011537600.1:n.*68T=
NM_001320974.2:c.1101+2887T= (COX15)	NP_001307903.1:n.1101+2887T=
NM_001320975.2:c.*1307T= (COX15)	NP_001307904.1:n.*1307T=
NM_001320976.2:c.*1126T= (COX15)	NP_001307905.1:n.*1126T=
NM_001372024.1:c.*345T= (COX15)	NP_001358953.1:n.*345T=
NM_001372025.1:c.*1126T= (COX15)	NP_001358954.1:n.*1126T=
NM_001372026.1:c.*1126T= (COX15)	NP_001358955.1:n.*1126T=
NM_001372027.1:c.*1230T= (COX15)	NP_001358956.1:n.*1230T=
NM_001372028.1:c.*553T= (COX15)	NP_001358957.1:n.*553T=
NM_004376.7:c.1120T= (COX15)	NP_004367.2:p.Phe374=
NM_078470.6:c.*1126T= (COX15) MANE Select	NP_510870.1:n.*1126T=
NR_164009.1:n.2199T= (COX15)