Canonical Allele Identifier: CA2610489318

Gene: COX15 CUTC

Linked Data

• gnomAD v4: 10-99713812-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713812A>C , CM000672.2:g.99713812A>C	GRCh38
NC_000010.10:g.101473569A>C , CM000672.1:g.101473569A>C	GRCh37
NC_000010.9:g.101463559A>C	NCBI36
NG_008986.1:g.23855T>G , LRG_406:g.23855T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*775T>G (COX15) MANE Select	ENSP00000016171.6:n.*775T>G
ENST00000649102.1:c.*460+2536T>G	ENSP00000497114.1:n.*460+2536T>G
ENST00000016171.5:c.*775T>G (COX15)	ENSP00000016171.5:n.*775T>G
ENST00000370483.9:c.1102-333T>G (COX15)	ENSP00000359514.5:n.1102-333T>G
ENST00000493385.5:n.117-9106A>C (CUTC)
NM_004376.5:c.1102-333T>G , LRG_406t2:c.1102-333T>G (COX15)	NP_004367.2:n.1102-333T>G
NM_078470.4:c.*775T>G , LRG_406t1:c.*775T>G (COX15)	NP_510870.1:n.*775T>G
XM_005269539.3:c.1101+2536T>G (COX15)	XP_005269596.1:n.1101+2536T>G
XM_006717633.2:c.*956T>G (COX15)	XP_006717696.1:n.*956T>G
XM_006717634.2:c.*49+2536T>G (COX15)	XP_006717697.1:n.*49+2536T>G
XM_011539298.1:c.*50-333T>G (COX15)	XP_011537600.1:n.*50-333T>G
NM_001320974.1:c.1101+2536T>G (COX15)	NP_001307903.1:n.1101+2536T>G
NM_001320975.1:c.*956T>G (COX15)	NP_001307904.1:n.*956T>G
NM_001320976.1:c.*775T>G (COX15)	NP_001307905.1:n.*775T>G
NM_004376.6:c.1102-333T>G (COX15)	NP_004367.2:n.1102-333T>G
NM_078470.5:c.*775T>G (COX15)	NP_510870.1:n.*775T>G
XM_006717634.3:c.*49+2536T>G (COX15)	XP_006717697.1:n.*49+2536T>G
XM_011539298.2:c.*50-333T>G (COX15)	XP_011537600.1:n.*50-333T>G
NM_001320974.2:c.1101+2536T>G (COX15)	NP_001307903.1:n.1101+2536T>G
NM_001320975.2:c.*956T>G (COX15)	NP_001307904.1:n.*956T>G
NM_001320976.2:c.*775T>G (COX15)	NP_001307905.1:n.*775T>G
NM_001372024.1:c.1254T>G (COX15)	NP_001358953.1:p.Tyr418Ter
NM_001372025.1:c.*775T>G (COX15)	NP_001358954.1:n.*775T>G
NM_001372026.1:c.*775T>G (COX15)	NP_001358955.1:n.*775T>G
NM_001372027.1:c.*879T>G (COX15)	NP_001358956.1:n.*879T>G
NM_001372028.1:c.*202T>G (COX15)	NP_001358957.1:n.*202T>G
NM_004376.7:c.1102-333T>G (COX15)	NP_004367.2:n.1102-333T>G
NM_078470.6:c.*775T>G (COX15) MANE Select	NP_510870.1:n.*775T>G
NR_164009.1:n.1848T>G (COX15)