Canonical Allele Identifier: CA1931452080

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713396G= , CM000672.2:g.99713396G=	GRCh38
NC_000010.10:g.101473153G= , CM000672.1:g.101473153G=	GRCh37
NC_000010.9:g.101463143G=	NCBI36
NG_008986.1:g.24271C= , LRG_406:g.24271C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*1191C= (COX15) MANE Select	ENSP00000016171.6:n.*1191C=
ENST00000649102.1:c.*460+2952C=	ENSP00000497114.1:n.*460+2952C=
ENST00000370483.9:c.*18C= (COX15)	ENSP00000359514.5:n.*18C=
ENST00000493385.5:n.117-9522G= (CUTC)
NM_004376.5:c.*18C= , LRG_406t2:c.*18C= (COX15)	NP_004367.2:n.*18C=
NM_078470.4:c.*1191C= , LRG_406t1:c.*1191C= (COX15)	NP_510870.1:n.*1191C=
XM_005269539.3:c.1101+2952C= (COX15)	XP_005269596.1:n.1101+2952C=
XM_006717633.2:c.*1372C= (COX15)	XP_006717696.1:n.*1372C=
XM_006717634.2:c.*49+2952C= (COX15)	XP_006717697.1:n.*49+2952C=
XM_011539298.1:c.*133C= (COX15)	XP_011537600.1:n.*133C=
NM_001320974.1:c.1101+2952C= (COX15)	NP_001307903.1:n.1101+2952C=
NM_001320975.1:c.*1372C= (COX15)	NP_001307904.1:n.*1372C=
NM_001320976.1:c.*1191C= (COX15)	NP_001307905.1:n.*1191C=
NM_004376.6:c.*18C= (COX15)	NP_004367.2:n.*18C=
NM_078470.5:c.*1191C= (COX15)	NP_510870.1:n.*1191C=
XM_006717634.3:c.*49+2952C= (COX15)	XP_006717697.1:n.*49+2952C=
XM_011539298.2:c.*133C= (COX15)	XP_011537600.1:n.*133C=
NM_001320974.2:c.1101+2952C= (COX15)	NP_001307903.1:n.1101+2952C=
NM_001320975.2:c.*1372C= (COX15)	NP_001307904.1:n.*1372C=
NM_001320976.2:c.*1191C= (COX15)	NP_001307905.1:n.*1191C=
NM_001372024.1:c.*410C= (COX15)	NP_001358953.1:n.*410C=
NM_001372025.1:c.*1191C= (COX15)	NP_001358954.1:n.*1191C=
NM_001372026.1:c.*1191C= (COX15)	NP_001358955.1:n.*1191C=
NM_001372027.1:c.*1295C= (COX15)	NP_001358956.1:n.*1295C=
NM_001372028.1:c.*618C= (COX15)	NP_001358957.1:n.*618C=
NM_004376.7:c.*18C= (COX15)	NP_004367.2:n.*18C=
NM_078470.6:c.*1191C= (COX15) MANE Select	NP_510870.1:n.*1191C=
NR_164009.1:n.2264C= (COX15)