Canonical Allele Identifier: CA1931452026

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713315A= , CM000672.2:g.99713315A=	GRCh38
NC_000010.10:g.101473072A= , CM000672.1:g.101473072A=	GRCh37
NC_000010.9:g.101463062A=	NCBI36
NG_008986.1:g.24352T= , LRG_406:g.24352T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*1272T= (COX15) MANE Select	ENSP00000016171.6:n.*1272T=
ENST00000649102.1:c.*460+3033T=	ENSP00000497114.1:n.*460+3033T=
ENST00000370483.9:c.*99T= (COX15)	ENSP00000359514.5:n.*99T=
ENST00000493385.5:n.117-9603A= (CUTC)
NM_004376.5:c.*99T= , LRG_406t2:c.*99T= (COX15)	NP_004367.2:n.*99T=
NM_078470.4:c.*1272T= , LRG_406t1:c.*1272T= (COX15)	NP_510870.1:n.*1272T=
XM_005269539.3:c.1101+3033T= (COX15)	XP_005269596.1:n.1101+3033T=
XM_006717633.2:c.*1453T= (COX15)	XP_006717696.1:n.*1453T=
XM_006717634.2:c.*49+3033T= (COX15)	XP_006717697.1:n.*49+3033T=
NM_001320974.1:c.1101+3033T= (COX15)	NP_001307903.1:n.1101+3033T=
NM_001320975.1:c.*1453T= (COX15)	NP_001307904.1:n.*1453T=
NM_001320976.1:c.*1272T= (COX15)	NP_001307905.1:n.*1272T=
NM_004376.6:c.*99T= (COX15)	NP_004367.2:n.*99T=
NM_078470.5:c.*1272T= (COX15)	NP_510870.1:n.*1272T=
XM_006717634.3:c.*49+3033T= (COX15)	XP_006717697.1:n.*49+3033T=
XM_011539298.2:c.*214T= (COX15)	XP_011537600.1:n.*214T=
NM_001320974.2:c.1101+3033T= (COX15)	NP_001307903.1:n.1101+3033T=
NM_001320975.2:c.*1453T= (COX15)	NP_001307904.1:n.*1453T=
NM_001320976.2:c.*1272T= (COX15)	NP_001307905.1:n.*1272T=
NM_001372024.1:c.*491T= (COX15)	NP_001358953.1:n.*491T=
NM_001372025.1:c.*1272T= (COX15)	NP_001358954.1:n.*1272T=
NM_001372026.1:c.*1272T= (COX15)	NP_001358955.1:n.*1272T=
NM_001372027.1:c.*1376T= (COX15)	NP_001358956.1:n.*1376T=
NM_001372028.1:c.*699T= (COX15)	NP_001358957.1:n.*699T=
NM_004376.7:c.*99T= (COX15)	NP_004367.2:n.*99T=
NM_078470.6:c.*1272T= (COX15) MANE Select	NP_510870.1:n.*1272T=
NR_164009.1:n.2345T= (COX15)