Canonical Allele Identifier: CA1931452074

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713387G= , CM000672.2:g.99713387G=	GRCh38
NC_000010.10:g.101473144G= , CM000672.1:g.101473144G=	GRCh37
NC_000010.9:g.101463134G=	NCBI36
NG_008986.1:g.24280C= , LRG_406:g.24280C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*1200C= (COX15) MANE Select	ENSP00000016171.6:n.*1200C=
ENST00000649102.1:c.*460+2961C=	ENSP00000497114.1:n.*460+2961C=
ENST00000370483.9:c.*27C= (COX15)	ENSP00000359514.5:n.*27C=
ENST00000493385.5:n.117-9531G= (CUTC)
NM_004376.5:c.*27C= , LRG_406t2:c.*27C= (COX15)	NP_004367.2:n.*27C=
NM_078470.4:c.*1200C= , LRG_406t1:c.*1200C= (COX15)	NP_510870.1:n.*1200C=
XM_005269539.3:c.1101+2961C= (COX15)	XP_005269596.1:n.1101+2961C=
XM_006717633.2:c.*1381C= (COX15)	XP_006717696.1:n.*1381C=
XM_006717634.2:c.*49+2961C= (COX15)	XP_006717697.1:n.*49+2961C=
NM_001320974.1:c.1101+2961C= (COX15)	NP_001307903.1:n.1101+2961C=
NM_001320975.1:c.*1381C= (COX15)	NP_001307904.1:n.*1381C=
NM_001320976.1:c.*1200C= (COX15)	NP_001307905.1:n.*1200C=
NM_004376.6:c.*27C= (COX15)	NP_004367.2:n.*27C=
NM_078470.5:c.*1200C= (COX15)	NP_510870.1:n.*1200C=
XM_006717634.3:c.*49+2961C= (COX15)	XP_006717697.1:n.*49+2961C=
XM_011539298.2:c.*142C= (COX15)	XP_011537600.1:n.*142C=
NM_001320974.2:c.1101+2961C= (COX15)	NP_001307903.1:n.1101+2961C=
NM_001320975.2:c.*1381C= (COX15)	NP_001307904.1:n.*1381C=
NM_001320976.2:c.*1200C= (COX15)	NP_001307905.1:n.*1200C=
NM_001372024.1:c.*419C= (COX15)	NP_001358953.1:n.*419C=
NM_001372025.1:c.*1200C= (COX15)	NP_001358954.1:n.*1200C=
NM_001372026.1:c.*1200C= (COX15)	NP_001358955.1:n.*1200C=
NM_001372027.1:c.*1304C= (COX15)	NP_001358956.1:n.*1304C=
NM_001372028.1:c.*627C= (COX15)	NP_001358957.1:n.*627C=
NM_004376.7:c.*27C= (COX15)	NP_004367.2:n.*27C=
NM_078470.6:c.*1200C= (COX15) MANE Select	NP_510870.1:n.*1200C=
NR_164009.1:n.2273C= (COX15)