Canonical Allele Identifier: CA471131726

Gene: COX15 CUTC

Linked Data

• MyVariant Identifiers: chr10:g.101474389A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99714632A>T , CM000672.2:g.99714632A>T	GRCh38
NC_000010.10:g.101474389A>T , CM000672.1:g.101474389A>T	GRCh37
NC_000010.9:g.101464379A>T	NCBI36
NG_008986.1:g.23035T>A , LRG_406:g.23035T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000016171.6:c.1188T>A (COX15) MANE Select	ENSP00000016171.6:p.Thr396=
ENST00000649102.1:c.*460+1716T>A	ENSP00000497114.1:n.*460+1716T>A
ENST00000016171.5:c.1188T>A (COX15)	ENSP00000016171.5:p.Thr396=
ENST00000370483.9:c.1102-1153T>A (COX15)	ENSP00000359514.5:n.1102-1153T>A
ENST00000493385.5:n.117-8286A>T (CUTC)
NM_004376.5:c.1102-1153T>A , LRG_406t2:c.1102-1153T>A (COX15)	NP_004367.2:n.1102-1153T>A
NM_078470.4:c.1188T>A , LRG_406t1:c.1188T>A (COX15)	NP_510870.1:p.Thr396=
XM_005269539.3:c.1101+1716T>A (COX15)	XP_005269596.1:n.1101+1716T>A
XM_006717633.2:c.*136T>A (COX15)	XP_006717696.1:n.*136T>A
XM_006717634.2:c.*49+1716T>A (COX15)	XP_006717697.1:n.*49+1716T>A
XM_011539298.1:c.*50-1153T>A (COX15)	XP_011537600.1:n.*50-1153T>A
NM_001320974.1:c.1101+1716T>A (COX15)	NP_001307903.1:n.1101+1716T>A
NM_001320975.1:c.*136T>A (COX15)	NP_001307904.1:n.*136T>A
NM_001320976.1:c.651T>A (COX15)	NP_001307905.1:p.Thr217=
NM_004376.6:c.1102-1153T>A (COX15)	NP_004367.2:n.1102-1153T>A
NM_078470.5:c.1188T>A (COX15)	NP_510870.1:p.Thr396=
XM_006717634.3:c.*49+1716T>A (COX15)	XP_006717697.1:n.*49+1716T>A
XM_011539298.2:c.*50-1153T>A (COX15)	XP_011537600.1:n.*50-1153T>A
NM_001320974.2:c.1101+1716T>A (COX15)	NP_001307903.1:n.1101+1716T>A
NM_001320975.2:c.*136T>A (COX15)	NP_001307904.1:n.*136T>A
NM_001320976.2:c.651T>A (COX15)	NP_001307905.1:p.Thr217=
NM_001372024.1:c.1102-668T>A (COX15)	NP_001358953.1:n.1102-668T>A
NM_001372025.1:c.1206T>A (COX15)	NP_001358954.1:p.Thr402=
NM_001372026.1:c.1161T>A (COX15)	NP_001358955.1:p.Thr387=
NM_001372027.1:c.*59T>A (COX15)	NP_001358956.1:n.*59T>A
NM_001372028.1:c.*50-668T>A (COX15)	NP_001358957.1:n.*50-668T>A
NM_004376.7:c.1102-1153T>A (COX15)	NP_004367.2:n.1102-1153T>A
NM_078470.6:c.1188T>A (COX15) MANE Select	NP_510870.1:p.Thr396=
NR_164009.1:n.1028T>A (COX15)