Canonical Allele Identifier: CA405957668

Gene: COQ8B

Linked Data

• gnomAD v4: 19-40692246-C-A
• COSMIC: COSM6394926 ; COSM6394927
• MyVariant Identifiers: chr19:g.41198151C>A (hg19) ; chr19:g.40692246C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40692246C>A , CM000681.2:g.40692246C>A	GRCh38
NC_000019.9:g.41198151C>A , CM000681.1:g.41198151C>A	GRCh37
NC_000019.8:g.45889991C>A	NCBI36
NG_027800.1:g.29640G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.1424G>T MANE Select	ENSP00000315118.3:p.Arg475Leu
ENST00000593724.2:n.3247G>T
ENST00000594490.6:c.1346G>T	ENSP00000471310.2:p.Arg449Leu
ENST00000594720.6:c.1424G>T	ENSP00000470876.2:p.Arg475Leu
ENST00000596455.6:n.1716G>T
ENST00000601967.6:c.1424G>T	ENSP00000470916.2:p.Arg475Leu
ENST00000676555.1:c.*849G>T	ENSP00000503387.1:n.*849G>T
ENST00000676578.1:c.*1166G>T	ENSP00000504076.1:n.*1166G>T
ENST00000676960.1:n.1549G>T
ENST00000676962.1:n.1703G>T
ENST00000677018.1:c.1424G>T	ENSP00000503480.1:p.Arg475Leu
ENST00000677039.1:n.3627G>T
ENST00000677399.1:n.1866G>T
ENST00000677496.1:c.1097G>T	ENSP00000504773.1:p.Arg366Leu
ENST00000677517.1:c.1097G>T	ENSP00000503519.1:p.Arg366Leu
ENST00000677633.1:c.*847G>T	ENSP00000503645.1:n.*847G>T
ENST00000677800.1:c.*4528G>T	ENSP00000503794.1:n.*4528G>T
ENST00000678057.1:c.*988G>T	ENSP00000503762.1:n.*988G>T
ENST00000678119.1:n.1618G>T
ENST00000678166.1:n.1567G>T
ENST00000678312.1:n.1761G>T
ENST00000678316.1:c.*847G>T	ENSP00000504112.1:n.*847G>T
ENST00000678371.1:n.1874G>T
ENST00000678404.1:c.1424G>T	ENSP00000503944.1:p.Arg475Leu
ENST00000678419.1:c.1424G>T	ENSP00000504085.1:p.Arg475Leu
ENST00000678433.1:n.1780G>T
ENST00000678467.1:c.1424G>T	ENSP00000504072.1:p.Arg475Leu
ENST00000678569.1:c.*409G>T	ENSP00000504261.1:n.*409G>T
ENST00000678961.1:n.1779G>T
ENST00000679002.1:n.1603G>T
ENST00000679012.1:c.980G>T	ENSP00000504446.1:p.Arg327Leu
ENST00000679070.1:c.*843G>T	ENSP00000503759.1:n.*843G>T
ENST00000679130.1:c.1424G>T	ENSP00000504845.1:p.Arg475Leu
ENST00000679315.1:c.*1254G>T	ENSP00000503065.1:n.*1254G>T
ENST00000243583.10:c.1301G>T	ENSP00000243583.5:p.Arg434Leu
ENST00000324464.7:c.1424G>T	ENSP00000315118.3:p.Arg475Leu
ENST00000593724.1:n.1539G>T
NM_001142555.2:c.1301G>T	NP_001136027.1:p.Arg434Leu
NM_024876.3:c.1424G>T	NP_079152.3:p.Arg475Leu
XM_005259270.3:c.1586G>T	XP_005259327.2:p.Arg529Leu
XM_005259271.3:c.1424G>T	XP_005259328.1:p.Arg475Leu
XM_005259272.3:c.1424G>T	XP_005259329.1:p.Arg475Leu
XM_005259273.3:c.1424G>T	XP_005259330.1:p.Arg475Leu
XM_006723392.2:c.1424G>T	XP_006723455.1:p.Arg475Leu
XM_006723393.2:c.1424G>T	XP_006723456.1:p.Arg475Leu
XM_011527334.1:c.1424G>T	XP_011525636.1:p.Arg475Leu
XM_011527335.1:c.1283G>T	XP_011525637.1:p.Arg428Leu
XM_011527336.1:c.1454G>T	XP_011525638.1:p.Arg485Leu
XM_011527337.1:c.1424G>T	XP_011525639.1:p.Arg475Leu
XM_011527338.1:c.1424G>T	XP_011525640.1:p.Arg475Leu
NM_024876.4:c.1424G>T MANE Select	NP_079152.3:p.Arg475Leu
NM_001142555.3:c.1301G>T	NP_001136027.1:p.Arg434Leu