Canonical Allele Identifier: CA2585172114

Gene: COQ8B

Linked Data

• gnomAD v4: 19-40692018-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40692019dup , CM000681.2:g.40692019dup	GRCh38
NC_000019.9:g.41197924dup , CM000681.1:g.41197924dup	GRCh37
NC_000019.8:g.45889764dup	NCBI36
NG_027800.1:g.29867dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.*16dup MANE Select	ENSP00000315118.3:n.*16dup
ENST00000593724.2:n.3474dup
ENST00000594490.6:c.*16dup	ENSP00000471310.2:n.*16dup
ENST00000594720.6:c.*16dup	ENSP00000470876.2:n.*16dup
ENST00000596455.6:n.1943dup
ENST00000601967.6:c.*16dup	ENSP00000470916.2:n.*16dup
ENST00000676555.1:c.*1076dup	ENSP00000503387.1:n.*1076dup
ENST00000676578.1:c.*1393dup	ENSP00000504076.1:n.*1393dup
ENST00000676960.1:n.1776dup
ENST00000676962.1:n.1930dup
ENST00000677018.1:c.*16dup	ENSP00000503480.1:n.*16dup
ENST00000677039.1:n.3854dup
ENST00000677399.1:n.2093dup
ENST00000677496.1:c.*16dup	ENSP00000504773.1:n.*16dup
ENST00000677517.1:c.*16dup	ENSP00000503519.1:n.*16dup
ENST00000677633.1:c.*1074dup	ENSP00000503645.1:n.*1074dup
ENST00000677800.1:c.*4755dup	ENSP00000503794.1:n.*4755dup
ENST00000678057.1:c.*1215dup	ENSP00000503762.1:n.*1215dup
ENST00000678119.1:n.1845dup
ENST00000678166.1:n.1794dup
ENST00000678312.1:n.1988dup
ENST00000678316.1:c.*1074dup	ENSP00000504112.1:n.*1074dup
ENST00000678371.1:n.2101dup
ENST00000678404.1:c.*16dup	ENSP00000503944.1:n.*16dup
ENST00000678419.1:c.*16dup	ENSP00000504085.1:n.*16dup
ENST00000678433.1:n.2007dup
ENST00000678467.1:c.*16dup	ENSP00000504072.1:n.*16dup
ENST00000678569.1:c.*636dup	ENSP00000504261.1:n.*636dup
ENST00000678961.1:n.2006dup
ENST00000679002.1:n.1830dup
ENST00000679012.1:c.*16dup	ENSP00000504446.1:n.*16dup
ENST00000679070.1:c.*1070dup	ENSP00000503759.1:n.*1070dup
ENST00000679130.1:c.*16dup	ENSP00000504845.1:n.*16dup
ENST00000679315.1:c.*1481dup	ENSP00000503065.1:n.*1481dup
ENST00000243583.10:c.*16dup	ENSP00000243583.5:n.*16dup
ENST00000324464.7:c.*16dup	ENSP00000315118.3:n.*16dup
ENST00000593724.1:n.1766dup
NM_001142555.2:c.*16dup	NP_001136027.1:n.*16dup
NM_024876.3:c.*16dup	NP_079152.3:n.*16dup
XM_005259270.3:c.*16dup	XP_005259327.2:n.*16dup
XM_005259271.3:c.*16dup	XP_005259328.1:n.*16dup
XM_005259272.3:c.*16dup	XP_005259329.1:n.*16dup
XM_005259273.3:c.*16dup	XP_005259330.1:n.*16dup
XM_006723392.2:c.*16dup	XP_006723455.1:n.*16dup
XM_006723393.2:c.*16dup	XP_006723456.1:n.*16dup
XM_011527334.1:c.*16dup	XP_011525636.1:n.*16dup
XM_011527335.1:c.*16dup	XP_011525637.1:n.*16dup
XM_011527336.1:c.*16dup	XP_011525638.1:n.*16dup
XM_011527337.1:c.*16dup	XP_011525639.1:n.*16dup
XM_011527338.1:c.*16dup	XP_011525640.1:n.*16dup
NM_024876.4:c.*16dup MANE Select	NP_079152.3:n.*16dup
NM_001142555.3:c.*16dup	NP_001136027.1:n.*16dup