Canonical Allele Identifier: CA1931452090

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713403C= , CM000672.2:g.99713403C=	GRCh38
NC_000010.10:g.101473160C= , CM000672.1:g.101473160C=	GRCh37
NC_000010.9:g.101463150C=	NCBI36
NG_008986.1:g.24264G= , LRG_406:g.24264G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*1184G= (COX15) MANE Select	ENSP00000016171.6:n.*1184G=
ENST00000649102.1:c.*460+2945G=	ENSP00000497114.1:n.*460+2945G=
ENST00000370483.9:c.*11G= (COX15)	ENSP00000359514.5:n.*11G=
ENST00000493385.5:n.117-9515C= (CUTC)
NM_004376.5:c.*11G= , LRG_406t2:c.*11G= (COX15)	NP_004367.2:n.*11G=
NM_078470.4:c.*1184G= , LRG_406t1:c.*1184G= (COX15)	NP_510870.1:n.*1184G=
XM_005269539.3:c.1101+2945G= (COX15)	XP_005269596.1:n.1101+2945G=
XM_006717633.2:c.*1365G= (COX15)	XP_006717696.1:n.*1365G=
XM_006717634.2:c.*49+2945G= (COX15)	XP_006717697.1:n.*49+2945G=
XM_011539298.1:c.*126G= (COX15)	XP_011537600.1:n.*126G=
NM_001320974.1:c.1101+2945G= (COX15)	NP_001307903.1:n.1101+2945G=
NM_001320975.1:c.*1365G= (COX15)	NP_001307904.1:n.*1365G=
NM_001320976.1:c.*1184G= (COX15)	NP_001307905.1:n.*1184G=
NM_004376.6:c.*11G= (COX15)	NP_004367.2:n.*11G=
NM_078470.5:c.*1184G= (COX15)	NP_510870.1:n.*1184G=
XM_006717634.3:c.*49+2945G= (COX15)	XP_006717697.1:n.*49+2945G=
XM_011539298.2:c.*126G= (COX15)	XP_011537600.1:n.*126G=
NM_001320974.2:c.1101+2945G= (COX15)	NP_001307903.1:n.1101+2945G=
NM_001320975.2:c.*1365G= (COX15)	NP_001307904.1:n.*1365G=
NM_001320976.2:c.*1184G= (COX15)	NP_001307905.1:n.*1184G=
NM_001372024.1:c.*403G= (COX15)	NP_001358953.1:n.*403G=
NM_001372025.1:c.*1184G= (COX15)	NP_001358954.1:n.*1184G=
NM_001372026.1:c.*1184G= (COX15)	NP_001358955.1:n.*1184G=
NM_001372027.1:c.*1288G= (COX15)	NP_001358956.1:n.*1288G=
NM_001372028.1:c.*611G= (COX15)	NP_001358957.1:n.*611G=
NM_004376.7:c.*11G= (COX15)	NP_004367.2:n.*11G=
NM_078470.6:c.*1184G= (COX15) MANE Select	NP_510870.1:n.*1184G=
NR_164009.1:n.2257G= (COX15)