Canonical Allele Identifier: CA2585171934

Gene: COQ8B

Linked Data

• gnomAD v4: 19-40691853-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40691854del , CM000681.2:g.40691854del	GRCh38
NC_000019.9:g.41197759del , CM000681.1:g.41197759del	GRCh37
NC_000019.8:g.45889599del	NCBI36
NG_027800.1:g.30032del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.*181del MANE Select	ENSP00000315118.3:n.*181del
ENST00000593724.2:n.3639del
ENST00000594490.6:c.*181del	ENSP00000471310.2:n.*181del
ENST00000594720.6:c.*181del	ENSP00000470876.2:n.*181del
ENST00000596455.6:n.2108del
ENST00000601967.6:c.*181del	ENSP00000470916.2:n.*181del
ENST00000676555.1:c.*1241del	ENSP00000503387.1:n.*1241del
ENST00000676578.1:c.*1558del	ENSP00000504076.1:n.*1558del
ENST00000676960.1:n.1941del
ENST00000676962.1:n.2095del
ENST00000677018.1:c.*181del	ENSP00000503480.1:n.*181del
ENST00000677039.1:n.4019del
ENST00000677399.1:n.2258del
ENST00000677496.1:c.*181del	ENSP00000504773.1:n.*181del
ENST00000677517.1:c.*181del	ENSP00000503519.1:n.*181del
ENST00000677633.1:c.*1239del	ENSP00000503645.1:n.*1239del
ENST00000677800.1:c.*4920del	ENSP00000503794.1:n.*4920del
ENST00000678057.1:c.*1380del	ENSP00000503762.1:n.*1380del
ENST00000678119.1:n.2010del
ENST00000678166.1:n.1959del
ENST00000678312.1:n.2153del
ENST00000678316.1:c.*1239del	ENSP00000504112.1:n.*1239del
ENST00000678371.1:n.2266del
ENST00000678404.1:c.*181del	ENSP00000503944.1:n.*181del
ENST00000678419.1:c.*181del	ENSP00000504085.1:n.*181del
ENST00000678433.1:n.2172del
ENST00000678467.1:c.*181del	ENSP00000504072.1:n.*181del
ENST00000678569.1:c.*801del	ENSP00000504261.1:n.*801del
ENST00000678961.1:n.2171del
ENST00000679002.1:n.1995del
ENST00000679012.1:c.*181del	ENSP00000504446.1:n.*181del
ENST00000679070.1:c.*1235del	ENSP00000503759.1:n.*1235del
ENST00000679130.1:c.*181del	ENSP00000504845.1:n.*181del
ENST00000679315.1:c.*1646del	ENSP00000503065.1:n.*1646del
ENST00000243583.10:c.*181del	ENSP00000243583.5:n.*181del
ENST00000324464.7:c.*181del	ENSP00000315118.3:n.*181del
ENST00000593724.1:n.1931del
NM_001142555.2:c.*181del	NP_001136027.1:n.*181del
NM_024876.3:c.*181del	NP_079152.3:n.*181del
XM_005259270.3:c.*181del	XP_005259327.2:n.*181del
XM_005259271.3:c.*181del	XP_005259328.1:n.*181del
XM_005259272.3:c.*181del	XP_005259329.1:n.*181del
XM_005259273.3:c.*181del	XP_005259330.1:n.*181del
XM_006723392.2:c.*181del	XP_006723455.1:n.*181del
XM_006723393.2:c.*181del	XP_006723456.1:n.*181del
XM_011527334.1:c.*181del	XP_011525636.1:n.*181del
XM_011527335.1:c.*181del	XP_011525637.1:n.*181del
XM_011527336.1:c.*181del	XP_011525638.1:n.*181del
XM_011527337.1:c.*181del	XP_011525639.1:n.*181del
XM_011527338.1:c.*181del	XP_011525640.1:n.*181del
NM_024876.4:c.*181del MANE Select	NP_079152.3:n.*181del
NM_001142555.3:c.*181del	NP_001136027.1:n.*181del