Canonical Allele Identifier: CA405957864

Gene: COQ8B

Linked Data

• MyVariant Identifiers: chr19:g.41198204A>T (hg19) ; chr19:g.40692299A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40692299A>T , CM000681.2:g.40692299A>T	GRCh38
NC_000019.9:g.41198204A>T , CM000681.1:g.41198204A>T	GRCh37
NC_000019.8:g.45890044A>T	NCBI36
NG_027800.1:g.29587T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.1371T>A MANE Select	ENSP00000315118.3:p.Phe457Leu
ENST00000593724.2:n.3194T>A
ENST00000594490.6:c.1293T>A	ENSP00000471310.2:p.Phe431Leu
ENST00000594720.6:c.1371T>A	ENSP00000470876.2:p.Phe457Leu
ENST00000596455.6:n.1663T>A
ENST00000601967.6:c.1371T>A	ENSP00000470916.2:p.Phe457Leu
ENST00000676555.1:c.*796T>A	ENSP00000503387.1:n.*796T>A
ENST00000676578.1:c.*1113T>A	ENSP00000504076.1:n.*1113T>A
ENST00000676960.1:n.1496T>A
ENST00000676962.1:n.1650T>A
ENST00000677018.1:c.1371T>A	ENSP00000503480.1:p.Phe457Leu
ENST00000677039.1:n.3574T>A
ENST00000677399.1:n.1813T>A
ENST00000677496.1:c.1044T>A	ENSP00000504773.1:p.Phe348Leu
ENST00000677517.1:c.1044T>A	ENSP00000503519.1:p.Phe348Leu
ENST00000677633.1:c.*794T>A	ENSP00000503645.1:n.*794T>A
ENST00000677800.1:c.*4475T>A	ENSP00000503794.1:n.*4475T>A
ENST00000678057.1:c.*935T>A	ENSP00000503762.1:n.*935T>A
ENST00000678119.1:n.1565T>A
ENST00000678166.1:n.1514T>A
ENST00000678312.1:n.1708T>A
ENST00000678316.1:c.*794T>A	ENSP00000504112.1:n.*794T>A
ENST00000678371.1:n.1821T>A
ENST00000678404.1:c.1371T>A	ENSP00000503944.1:p.Phe457Leu
ENST00000678419.1:c.1371T>A	ENSP00000504085.1:p.Phe457Leu
ENST00000678433.1:n.1727T>A
ENST00000678467.1:c.1371T>A	ENSP00000504072.1:p.Phe457Leu
ENST00000678569.1:c.*356T>A	ENSP00000504261.1:n.*356T>A
ENST00000678961.1:n.1726T>A
ENST00000679002.1:n.1550T>A
ENST00000679012.1:c.927T>A	ENSP00000504446.1:p.Phe309Leu
ENST00000679070.1:c.*790T>A	ENSP00000503759.1:n.*790T>A
ENST00000679130.1:c.1371T>A	ENSP00000504845.1:p.Phe457Leu
ENST00000679315.1:c.*1201T>A	ENSP00000503065.1:n.*1201T>A
ENST00000243583.10:c.1248T>A	ENSP00000243583.5:p.Phe416Leu
ENST00000324464.7:c.1371T>A	ENSP00000315118.3:p.Phe457Leu
ENST00000593724.1:n.1486T>A
NM_001142555.2:c.1248T>A	NP_001136027.1:p.Phe416Leu
NM_024876.3:c.1371T>A	NP_079152.3:p.Phe457Leu
XM_005259270.3:c.1533T>A	XP_005259327.2:p.Phe511Leu
XM_005259271.3:c.1371T>A	XP_005259328.1:p.Phe457Leu
XM_005259272.3:c.1371T>A	XP_005259329.1:p.Phe457Leu
XM_005259273.3:c.1371T>A	XP_005259330.1:p.Phe457Leu
XM_006723392.2:c.1371T>A	XP_006723455.1:p.Phe457Leu
XM_006723393.2:c.1371T>A	XP_006723456.1:p.Phe457Leu
XM_011527334.1:c.1371T>A	XP_011525636.1:p.Phe457Leu
XM_011527335.1:c.1230T>A	XP_011525637.1:p.Phe410Leu
XM_011527336.1:c.1401T>A	XP_011525638.1:p.Phe467Leu
XM_011527337.1:c.1371T>A	XP_011525639.1:p.Phe457Leu
XM_011527338.1:c.1371T>A	XP_011525640.1:p.Phe457Leu
NM_024876.4:c.1371T>A MANE Select	NP_079152.3:p.Phe457Leu
NM_001142555.3:c.1248T>A	NP_001136027.1:p.Phe416Leu