Canonical Allele Identifier: CA1931452049

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713341G= , CM000672.2:g.99713341G=	GRCh38
NC_000010.10:g.101473098G= , CM000672.1:g.101473098G=	GRCh37
NC_000010.9:g.101463088G=	NCBI36
NG_008986.1:g.24326C= , LRG_406:g.24326C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*1246C= (COX15) MANE Select	ENSP00000016171.6:n.*1246C=
ENST00000649102.1:c.*460+3007C=	ENSP00000497114.1:n.*460+3007C=
ENST00000370483.9:c.*73C= (COX15)	ENSP00000359514.5:n.*73C=
ENST00000493385.5:n.117-9577G= (CUTC)
NM_004376.5:c.*73C= , LRG_406t2:c.*73C= (COX15)	NP_004367.2:n.*73C=
NM_078470.4:c.*1246C= , LRG_406t1:c.*1246C= (COX15)	NP_510870.1:n.*1246C=
XM_005269539.3:c.1101+3007C= (COX15)	XP_005269596.1:n.1101+3007C=
XM_006717633.2:c.*1427C= (COX15)	XP_006717696.1:n.*1427C=
XM_006717634.2:c.*49+3007C= (COX15)	XP_006717697.1:n.*49+3007C=
NM_001320974.1:c.1101+3007C= (COX15)	NP_001307903.1:n.1101+3007C=
NM_001320975.1:c.*1427C= (COX15)	NP_001307904.1:n.*1427C=
NM_001320976.1:c.*1246C= (COX15)	NP_001307905.1:n.*1246C=
NM_004376.6:c.*73C= (COX15)	NP_004367.2:n.*73C=
NM_078470.5:c.*1246C= (COX15)	NP_510870.1:n.*1246C=
XM_006717634.3:c.*49+3007C= (COX15)	XP_006717697.1:n.*49+3007C=
XM_011539298.2:c.*188C= (COX15)	XP_011537600.1:n.*188C=
NM_001320974.2:c.1101+3007C= (COX15)	NP_001307903.1:n.1101+3007C=
NM_001320975.2:c.*1427C= (COX15)	NP_001307904.1:n.*1427C=
NM_001320976.2:c.*1246C= (COX15)	NP_001307905.1:n.*1246C=
NM_001372024.1:c.*465C= (COX15)	NP_001358953.1:n.*465C=
NM_001372025.1:c.*1246C= (COX15)	NP_001358954.1:n.*1246C=
NM_001372026.1:c.*1246C= (COX15)	NP_001358955.1:n.*1246C=
NM_001372027.1:c.*1350C= (COX15)	NP_001358956.1:n.*1350C=
NM_001372028.1:c.*673C= (COX15)	NP_001358957.1:n.*673C=
NM_004376.7:c.*73C= (COX15)	NP_004367.2:n.*73C=
NM_078470.6:c.*1246C= (COX15) MANE Select	NP_510870.1:n.*1246C=
NR_164009.1:n.2319C= (COX15)