Canonical Allele Identifier: CA2336101978
Gene: COQ8B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40692073G= , CM000681.2:g.40692073G= GRCh38
NC_000019.9:g.41197978G= , CM000681.1:g.41197978G= GRCh37
NC_000019.8:g.45889818G= NCBI36
NG_027800.1:g.29813C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324464.8:c.1597C= MANE Select ENSP00000315118.3:p.Leu533=
ENST00000593724.2:n.3420C=
ENST00000594490.6:c.1519C= ENSP00000471310.2:p.Leu507=
ENST00000594720.6:c.1597C= ENSP00000470876.2:p.Leu533=
ENST00000596455.6:n.1889C=
ENST00000601967.6:c.1597C= ENSP00000470916.2:p.Leu533=
ENST00000676555.1:c.*1022C= ENSP00000503387.1:n.*1022C=
ENST00000676578.1:c.*1339C= ENSP00000504076.1:n.*1339C=
ENST00000676960.1:n.1722C=
ENST00000676962.1:n.1876C=
ENST00000677018.1:c.1597C= ENSP00000503480.1:p.Leu533=
ENST00000677039.1:n.3800C=
ENST00000677399.1:n.2039C=
ENST00000677496.1:c.1270C= ENSP00000504773.1:p.Leu424=
ENST00000677517.1:c.1270C= ENSP00000503519.1:p.Leu424=
ENST00000677633.1:c.*1020C= ENSP00000503645.1:n.*1020C=
ENST00000677800.1:c.*4701C= ENSP00000503794.1:n.*4701C=
ENST00000678057.1:c.*1161C= ENSP00000503762.1:n.*1161C=
ENST00000678119.1:n.1791C=
ENST00000678166.1:n.1740C=
ENST00000678312.1:n.1934C=
ENST00000678316.1:c.*1020C= ENSP00000504112.1:n.*1020C=
ENST00000678371.1:n.2047C=
ENST00000678404.1:c.1597C= ENSP00000503944.1:p.Leu533=
ENST00000678419.1:c.1597C= ENSP00000504085.1:p.Leu533=
ENST00000678433.1:n.1953C=
ENST00000678467.1:c.1597C= ENSP00000504072.1:p.Leu533=
ENST00000678569.1:c.*582C= ENSP00000504261.1:n.*582C=
ENST00000678961.1:n.1952C=
ENST00000679002.1:n.1776C=
ENST00000679012.1:c.1153C= ENSP00000504446.1:p.Leu385=
ENST00000679070.1:c.*1016C= ENSP00000503759.1:n.*1016C=
ENST00000679130.1:c.1597C= ENSP00000504845.1:p.Leu533=
ENST00000679315.1:c.*1427C= ENSP00000503065.1:n.*1427C=
ENST00000243583.10:c.1474C= ENSP00000243583.5:p.Leu492=
ENST00000324464.7:c.1597C= ENSP00000315118.3:p.Leu533=
ENST00000593724.1:n.1712C=
NM_001142555.2:c.1474C= NP_001136027.1:p.Leu492=
NM_024876.3:c.1597C= NP_079152.3:p.Leu533=
XM_005259270.3:c.1759C= XP_005259327.2:p.Leu587=
XM_005259271.3:c.1597C= XP_005259328.1:p.Leu533=
XM_005259272.3:c.1597C= XP_005259329.1:p.Leu533=
XM_005259273.3:c.1597C= XP_005259330.1:p.Leu533=
XM_006723392.2:c.1597C= XP_006723455.1:p.Leu533=
XM_006723393.2:c.1597C= XP_006723456.1:p.Leu533=
XM_011527334.1:c.1597C= XP_011525636.1:p.Leu533=
XM_011527335.1:c.1456C= XP_011525637.1:p.Leu486=
XM_011527336.1:c.1627C= XP_011525638.1:p.Leu543=
XM_011527337.1:c.1597C= XP_011525639.1:p.Leu533=
XM_011527338.1:c.1597C= XP_011525640.1:p.Leu533=
NM_024876.4:c.1597C= MANE Select NP_079152.3:p.Leu533=
NM_001142555.3:c.1474C= NP_001136027.1:p.Leu492=