Canonical Allele Identifier: CA2789195130

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713575dup , CM000672.2:g.99713575dup	GRCh38
NC_000010.10:g.101473332dup , CM000672.1:g.101473332dup	GRCh37
NC_000010.9:g.101463322dup	NCBI36
NG_008986.1:g.24092dup , LRG_406:g.24092dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*1012dup (COX15) MANE Select	ENSP00000016171.6:n.*1012dup
ENST00000649102.1:c.*460+2773dup	ENSP00000497114.1:n.*460+2773dup
ENST00000016171.5:c.*1012dup (COX15)	ENSP00000016171.5:n.*1012dup
ENST00000370483.9:c.1102-96dup (COX15)	ENSP00000359514.5:n.1102-96dup
ENST00000493385.5:n.117-9343dup (CUTC)
NM_004376.5:c.1102-96dup , LRG_406t2:c.1102-96dup (COX15)	NP_004367.2:n.1102-96dup
NM_078470.4:c.*1012dup , LRG_406t1:c.*1012dup (COX15)	NP_510870.1:n.*1012dup
XM_005269539.3:c.1101+2773dup (COX15)	XP_005269596.1:n.1101+2773dup
XM_006717633.2:c.*1193dup (COX15)	XP_006717696.1:n.*1193dup
XM_006717634.2:c.*49+2773dup (COX15)	XP_006717697.1:n.*49+2773dup
XM_011539298.1:c.*50-96dup (COX15)	XP_011537600.1:n.*50-96dup
NM_001320974.1:c.1101+2773dup (COX15)	NP_001307903.1:n.1101+2773dup
NM_001320975.1:c.*1193dup (COX15)	NP_001307904.1:n.*1193dup
NM_001320976.1:c.*1012dup (COX15)	NP_001307905.1:n.*1012dup
NM_004376.6:c.1102-96dup (COX15)	NP_004367.2:n.1102-96dup
NM_078470.5:c.*1012dup (COX15)	NP_510870.1:n.*1012dup
XM_006717634.3:c.*49+2773dup (COX15)	XP_006717697.1:n.*49+2773dup
XM_011539298.2:c.*50-96dup (COX15)	XP_011537600.1:n.*50-96dup
NM_001320974.2:c.1101+2773dup (COX15)	NP_001307903.1:n.1101+2773dup
NM_001320975.2:c.*1193dup (COX15)	NP_001307904.1:n.*1193dup
NM_001320976.2:c.*1012dup (COX15)	NP_001307905.1:n.*1012dup
NM_001372024.1:c.*231dup (COX15)	NP_001358953.1:n.*231dup
NM_001372025.1:c.*1012dup (COX15)	NP_001358954.1:n.*1012dup
NM_001372026.1:c.*1012dup (COX15)	NP_001358955.1:n.*1012dup
NM_001372027.1:c.*1116dup (COX15)	NP_001358956.1:n.*1116dup
NM_001372028.1:c.*439dup (COX15)	NP_001358957.1:n.*439dup
NM_004376.7:c.1102-96dup (COX15)	NP_004367.2:n.1102-96dup
NM_078470.6:c.*1012dup (COX15) MANE Select	NP_510870.1:n.*1012dup
NR_164009.1:n.2085dup (COX15)