Canonical Allele Identifier: CA2336101969
Gene: COQ8B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40692038T= , CM000681.2:g.40692038T= GRCh38
NC_000019.9:g.41197943T= , CM000681.1:g.41197943T= GRCh37
NC_000019.8:g.45889783T= NCBI36
NG_027800.1:g.29848A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324464.8:c.1632A= MANE Select ENSP00000315118.3:p.Ser544=
ENST00000593724.2:n.3455A=
ENST00000594490.6:c.1554A= ENSP00000471310.2:p.Ser518=
ENST00000594720.6:c.1632A= ENSP00000470876.2:p.Ser544=
ENST00000596455.6:n.1924A=
ENST00000601967.6:c.1632A= ENSP00000470916.2:p.Ser544=
ENST00000676555.1:c.*1057A= ENSP00000503387.1:n.*1057A=
ENST00000676578.1:c.*1374A= ENSP00000504076.1:n.*1374A=
ENST00000676960.1:n.1757A=
ENST00000676962.1:n.1911A=
ENST00000677018.1:c.1632A= ENSP00000503480.1:p.Ser544=
ENST00000677039.1:n.3835A=
ENST00000677399.1:n.2074A=
ENST00000677496.1:c.1305A= ENSP00000504773.1:p.Ser435=
ENST00000677517.1:c.1305A= ENSP00000503519.1:p.Ser435=
ENST00000677633.1:c.*1055A= ENSP00000503645.1:n.*1055A=
ENST00000677800.1:c.*4736A= ENSP00000503794.1:n.*4736A=
ENST00000678057.1:c.*1196A= ENSP00000503762.1:n.*1196A=
ENST00000678119.1:n.1826A=
ENST00000678166.1:n.1775A=
ENST00000678312.1:n.1969A=
ENST00000678316.1:c.*1055A= ENSP00000504112.1:n.*1055A=
ENST00000678371.1:n.2082A=
ENST00000678404.1:c.1632A= ENSP00000503944.1:p.Ser544=
ENST00000678419.1:c.1632A= ENSP00000504085.1:p.Ser544=
ENST00000678433.1:n.1988A=
ENST00000678467.1:c.1632A= ENSP00000504072.1:p.Ser544=
ENST00000678569.1:c.*617A= ENSP00000504261.1:n.*617A=
ENST00000678961.1:n.1987A=
ENST00000679002.1:n.1811A=
ENST00000679012.1:c.1188A= ENSP00000504446.1:p.Ser396=
ENST00000679070.1:c.*1051A= ENSP00000503759.1:n.*1051A=
ENST00000679130.1:c.1632A= ENSP00000504845.1:p.Ser544=
ENST00000679315.1:c.*1462A= ENSP00000503065.1:n.*1462A=
ENST00000243583.10:c.1509A= ENSP00000243583.5:p.Ser503=
ENST00000324464.7:c.1632A= ENSP00000315118.3:p.Ser544=
ENST00000593724.1:n.1747A=
NM_001142555.2:c.1509A= NP_001136027.1:p.Ser503=
NM_024876.3:c.1632A= NP_079152.3:p.Ser544=
XM_005259270.3:c.1794A= XP_005259327.2:p.Ser598=
XM_005259271.3:c.1632A= XP_005259328.1:p.Ser544=
XM_005259272.3:c.1632A= XP_005259329.1:p.Ser544=
XM_005259273.3:c.1632A= XP_005259330.1:p.Ser544=
XM_006723392.2:c.1632A= XP_006723455.1:p.Ser544=
XM_006723393.2:c.1632A= XP_006723456.1:p.Ser544=
XM_011527334.1:c.1632A= XP_011525636.1:p.Ser544=
XM_011527335.1:c.1491A= XP_011525637.1:p.Ser497=
XM_011527336.1:c.1662A= XP_011525638.1:p.Ser554=
XM_011527337.1:c.1632A= XP_011525639.1:p.Ser544=
XM_011527338.1:c.1632A= XP_011525640.1:p.Ser544=
NM_024876.4:c.1632A= MANE Select NP_079152.3:p.Ser544=
NM_001142555.3:c.1509A= NP_001136027.1:p.Ser503=