Canonical Allele Identifier: CA378101083

Gene: COX15 CUTC

Linked Data

• gnomAD v4: 10-99713435-A-T
• MyVariant Identifiers: chr10:g.101473192A>T (hg19) ; chr10:g.99713435A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713435A>T , CM000672.2:g.99713435A>T	GRCh38
NC_000010.10:g.101473192A>T , CM000672.1:g.101473192A>T	GRCh37
NC_000010.9:g.101463182A>T	NCBI36
NG_008986.1:g.24232T>A , LRG_406:g.24232T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*1152T>A (COX15) MANE Select	ENSP00000016171.6:n.*1152T>A
ENST00000649102.1:c.*460+2913T>A	ENSP00000497114.1:n.*460+2913T>A
ENST00000370483.9:c.1146T>A (COX15)	ENSP00000359514.5:p.Asp382Glu
ENST00000493385.5:n.117-9483A>T (CUTC)
NM_004376.5:c.1146T>A , LRG_406t2:c.1146T>A (COX15)	NP_004367.2:p.Asp382Glu
NM_078470.4:c.*1152T>A , LRG_406t1:c.*1152T>A (COX15)	NP_510870.1:n.*1152T>A
XM_005269539.3:c.1101+2913T>A (COX15)	XP_005269596.1:n.1101+2913T>A
XM_006717633.2:c.*1333T>A (COX15)	XP_006717696.1:n.*1333T>A
XM_006717634.2:c.*49+2913T>A (COX15)	XP_006717697.1:n.*49+2913T>A
XM_011539298.1:c.*94T>A (COX15)	XP_011537600.1:n.*94T>A
NM_001320974.1:c.1101+2913T>A (COX15)	NP_001307903.1:n.1101+2913T>A
NM_001320975.1:c.*1333T>A (COX15)	NP_001307904.1:n.*1333T>A
NM_001320976.1:c.*1152T>A (COX15)	NP_001307905.1:n.*1152T>A
NM_004376.6:c.1146T>A (COX15)	NP_004367.2:p.Asp382Glu
NM_078470.5:c.*1152T>A (COX15)	NP_510870.1:n.*1152T>A
XM_006717634.3:c.*49+2913T>A (COX15)	XP_006717697.1:n.*49+2913T>A
XM_011539298.2:c.*94T>A (COX15)	XP_011537600.1:n.*94T>A
NM_001320974.2:c.1101+2913T>A (COX15)	NP_001307903.1:n.1101+2913T>A
NM_001320975.2:c.*1333T>A (COX15)	NP_001307904.1:n.*1333T>A
NM_001320976.2:c.*1152T>A (COX15)	NP_001307905.1:n.*1152T>A
NM_001372024.1:c.*371T>A (COX15)	NP_001358953.1:n.*371T>A
NM_001372025.1:c.*1152T>A (COX15)	NP_001358954.1:n.*1152T>A
NM_001372026.1:c.*1152T>A (COX15)	NP_001358955.1:n.*1152T>A
NM_001372027.1:c.*1256T>A (COX15)	NP_001358956.1:n.*1256T>A
NM_001372028.1:c.*579T>A (COX15)	NP_001358957.1:n.*579T>A
NM_004376.7:c.1146T>A (COX15)	NP_004367.2:p.Asp382Glu
NM_078470.6:c.*1152T>A (COX15) MANE Select	NP_510870.1:n.*1152T>A
NR_164009.1:n.2225T>A (COX15)