Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713808A= , CM000672.2:g.99713808A=	GRCh38
NC_000010.10:g.101473565A= , CM000672.1:g.101473565A=	GRCh37
NC_000010.9:g.101463555A=	NCBI36
NG_008986.1:g.23859T= , LRG_406:g.23859T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*779T= (COX15) MANE Select	ENSP00000016171.6:n.*779T=
ENST00000649102.1:c.*460+2540T=	ENSP00000497114.1:n.*460+2540T=
ENST00000016171.5:c.*779T= (COX15)	ENSP00000016171.5:n.*779T=
ENST00000370483.9:c.1102-329T= (COX15)	ENSP00000359514.5:n.1102-329T=
ENST00000493385.5:n.117-9110A= (CUTC)
NM_004376.5:c.1102-329T= , LRG_406t2:c.1102-329T= (COX15)	NP_004367.2:n.1102-329T=
NM_078470.4:c.779T= , LRG_406t1:c.779T= (COX15)	NP_510870.1:n.*779T=
XM_005269539.3:c.1101+2540T= (COX15)	XP_005269596.1:n.1101+2540T=
XM_006717633.2:c.*960T= (COX15)	XP_006717696.1:n.*960T=
XM_006717634.2:c.*49+2540T= (COX15)	XP_006717697.1:n.*49+2540T=
XM_011539298.1:c.*50-329T= (COX15)	XP_011537600.1:n.*50-329T=
NM_001320974.1:c.1101+2540T= (COX15)	NP_001307903.1:n.1101+2540T=
NM_001320975.1:c.*960T= (COX15)	NP_001307904.1:n.*960T=
NM_001320976.1:c.*779T= (COX15)	NP_001307905.1:n.*779T=
NM_004376.6:c.1102-329T= (COX15)	NP_004367.2:n.1102-329T=
NM_078470.5:c.*779T= (COX15)	NP_510870.1:n.*779T=
XM_006717634.3:c.*49+2540T= (COX15)	XP_006717697.1:n.*49+2540T=
XM_011539298.2:c.*50-329T= (COX15)	XP_011537600.1:n.*50-329T=
NM_001320974.2:c.1101+2540T= (COX15)	NP_001307903.1:n.1101+2540T=
NM_001320975.2:c.*960T= (COX15)	NP_001307904.1:n.*960T=
NM_001320976.2:c.*779T= (COX15)	NP_001307905.1:n.*779T=
NM_001372024.1:c.1258T= (COX15)	NP_001358953.1:p.Ter420=
NM_001372025.1:c.*779T= (COX15)	NP_001358954.1:n.*779T=
NM_001372026.1:c.*779T= (COX15)	NP_001358955.1:n.*779T=
NM_001372027.1:c.*883T= (COX15)	NP_001358956.1:n.*883T=
NM_001372028.1:c.*206T= (COX15)	NP_001358957.1:n.*206T=
NM_004376.7:c.1102-329T= (COX15)	NP_004367.2:n.1102-329T=
NM_078470.6:c.*779T= (COX15) MANE Select	NP_510870.1:n.*779T=
NR_164009.1:n.1852T= (COX15)