Canonical Allele Identifier: CA2585172766

Gene: COQ8B

Linked Data

• gnomAD v4: 19-40700224-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40700226dup , CM000681.2:g.40700226dup	GRCh38
NC_000019.9:g.41206131dup , CM000681.1:g.41206131dup	GRCh37
NC_000019.8:g.45897971dup	NCBI36
NG_027800.1:g.21661dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.1036-51dup MANE Select	ENSP00000315118.3:n.1036-51dup
ENST00000593724.2:n.2859-51dup
ENST00000594490.6:c.958-51dup	ENSP00000471310.2:n.958-51dup
ENST00000594720.6:c.1036-51dup	ENSP00000470876.2:n.1036-51dup
ENST00000596455.6:n.1328-51dup
ENST00000601967.6:c.1036-51dup	ENSP00000470916.2:n.1036-51dup
ENST00000676555.1:c.1036-51dup	ENSP00000503387.1:n.1036-51dup
ENST00000676578.1:c.*778-51dup	ENSP00000504076.1:n.*778-51dup
ENST00000676960.1:n.1161-51dup
ENST00000676962.1:n.1315-51dup
ENST00000677018.1:c.1036-51dup	ENSP00000503480.1:n.1036-51dup
ENST00000677039.1:n.3239-51dup
ENST00000677399.1:n.1478-51dup
ENST00000677496.1:c.709-51dup	ENSP00000504773.1:n.709-51dup
ENST00000677517.1:c.709-51dup	ENSP00000503519.1:n.709-51dup
ENST00000677633.1:c.*459-51dup	ENSP00000503645.1:n.*459-51dup
ENST00000677800.1:c.*4140-51dup	ENSP00000503794.1:n.*4140-51dup
ENST00000678057.1:c.*600-51dup	ENSP00000503762.1:n.*600-51dup
ENST00000678119.1:n.1230-51dup
ENST00000678166.1:n.1179-51dup
ENST00000678312.1:n.1373-51dup
ENST00000678316.1:c.*459-51dup	ENSP00000504112.1:n.*459-51dup
ENST00000678371.1:n.1486-51dup
ENST00000678404.1:c.1036-51dup	ENSP00000503944.1:n.1036-51dup
ENST00000678419.1:c.1036-51dup	ENSP00000504085.1:n.1036-51dup
ENST00000678433.1:n.1392-51dup
ENST00000678467.1:c.1036-51dup	ENSP00000504072.1:n.1036-51dup
ENST00000678569.1:c.*21-51dup	ENSP00000504261.1:n.*21-51dup
ENST00000678961.1:n.1391-51dup
ENST00000679002.1:n.1215-51dup
ENST00000679012.1:c.592-51dup	ENSP00000504446.1:n.592-51dup
ENST00000679070.1:c.*455-51dup	ENSP00000503759.1:n.*455-51dup
ENST00000679130.1:c.1036-51dup	ENSP00000504845.1:n.1036-51dup
ENST00000679315.1:c.*866-51dup	ENSP00000503065.1:n.*866-51dup
ENST00000243583.10:c.913-51dup	ENSP00000243583.5:n.913-51dup
ENST00000324464.7:c.1036-51dup	ENSP00000315118.3:n.1036-51dup
ENST00000593724.1:n.1151-51dup
NM_001142555.2:c.913-51dup	NP_001136027.1:n.913-51dup
NM_024876.3:c.1036-51dup	NP_079152.3:n.1036-51dup
XM_005259270.3:c.1198-51dup	XP_005259327.2:n.1198-51dup
XM_005259271.3:c.1036-51dup	XP_005259328.1:n.1036-51dup
XM_005259272.3:c.1036-51dup	XP_005259329.1:n.1036-51dup
XM_005259273.3:c.1036-51dup	XP_005259330.1:n.1036-51dup
XM_006723392.2:c.1036-51dup	XP_006723455.1:n.1036-51dup
XM_006723393.2:c.1036-51dup	XP_006723456.1:n.1036-51dup
XM_011527334.1:c.1036-51dup	XP_011525636.1:n.1036-51dup
XM_011527335.1:c.895-51dup	XP_011525637.1:n.895-51dup
XM_011527336.1:c.1066-51dup	XP_011525638.1:n.1066-51dup
XM_011527337.1:c.1036-51dup	XP_011525639.1:n.1036-51dup
XM_011527338.1:c.1036-51dup	XP_011525640.1:n.1036-51dup
NM_024876.4:c.1036-51dup MANE Select	NP_079152.3:n.1036-51dup
NM_001142555.3:c.913-51dup	NP_001136027.1:n.913-51dup