Canonical Allele Identifier: CA405960806

Gene: COQ8B

Linked Data

• MyVariant Identifiers: chr19:g.41206259G>C (hg19) ; chr19:g.40700354G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40700354G>C , CM000681.2:g.40700354G>C	GRCh38
NC_000019.9:g.41206259G>C , CM000681.1:g.41206259G>C	GRCh37
NC_000019.8:g.45898099G>C	NCBI36
NG_027800.1:g.21532C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.991C>G MANE Select	ENSP00000315118.3:p.Pro331Ala
ENST00000593724.2:n.2814C>G
ENST00000594490.6:c.913C>G	ENSP00000471310.2:p.Pro305Ala
ENST00000594720.6:c.991C>G	ENSP00000470876.2:p.Pro331Ala
ENST00000596455.6:n.1283C>G
ENST00000601967.6:c.991C>G	ENSP00000470916.2:p.Pro331Ala
ENST00000676555.1:c.991C>G	ENSP00000503387.1:p.Pro331Ala
ENST00000676578.1:c.*733C>G	ENSP00000504076.1:n.*733C>G
ENST00000676960.1:n.1116C>G
ENST00000676962.1:n.1270C>G
ENST00000677018.1:c.991C>G	ENSP00000503480.1:p.Pro331Ala
ENST00000677039.1:n.3194C>G
ENST00000677399.1:n.1433C>G
ENST00000677496.1:c.664C>G	ENSP00000504773.1:p.Pro222Ala
ENST00000677517.1:c.664C>G	ENSP00000503519.1:p.Pro222Ala
ENST00000677633.1:c.*414C>G	ENSP00000503645.1:n.*414C>G
ENST00000677800.1:c.*4095C>G	ENSP00000503794.1:n.*4095C>G
ENST00000678057.1:c.*555C>G	ENSP00000503762.1:n.*555C>G
ENST00000678119.1:n.1185C>G
ENST00000678166.1:n.1134C>G
ENST00000678312.1:n.1328C>G
ENST00000678316.1:c.*414C>G	ENSP00000504112.1:n.*414C>G
ENST00000678371.1:n.1441C>G
ENST00000678404.1:c.991C>G	ENSP00000503944.1:p.Pro331Ala
ENST00000678419.1:c.991C>G	ENSP00000504085.1:p.Pro331Ala
ENST00000678433.1:n.1347C>G
ENST00000678467.1:c.991C>G	ENSP00000504072.1:p.Pro331Ala
ENST00000678569.1:c.987C>G	ENSP00000504261.1:p.Ser329=
ENST00000678961.1:n.1346C>G
ENST00000679002.1:n.1170C>G
ENST00000679012.1:c.547C>G	ENSP00000504446.1:p.Pro183Ala
ENST00000679070.1:c.*410C>G	ENSP00000503759.1:n.*410C>G
ENST00000679130.1:c.991C>G	ENSP00000504845.1:p.Pro331Ala
ENST00000679315.1:c.*821C>G	ENSP00000503065.1:n.*821C>G
ENST00000243583.10:c.868C>G	ENSP00000243583.5:p.Pro290Ala
ENST00000324464.7:c.991C>G	ENSP00000315118.3:p.Pro331Ala
ENST00000593724.1:n.1106C>G
NM_001142555.2:c.868C>G	NP_001136027.1:p.Pro290Ala
NM_024876.3:c.991C>G	NP_079152.3:p.Pro331Ala
XM_005259270.3:c.1153C>G	XP_005259327.2:p.Pro385Ala
XM_005259271.3:c.991C>G	XP_005259328.1:p.Pro331Ala
XM_005259272.3:c.991C>G	XP_005259329.1:p.Pro331Ala
XM_005259273.3:c.991C>G	XP_005259330.1:p.Pro331Ala
XM_006723392.2:c.991C>G	XP_006723455.1:p.Pro331Ala
XM_006723393.2:c.991C>G	XP_006723456.1:p.Pro331Ala
XM_011527334.1:c.991C>G	XP_011525636.1:p.Pro331Ala
XM_011527335.1:c.850C>G	XP_011525637.1:p.Pro284Ala
XM_011527336.1:c.1021C>G	XP_011525638.1:p.Pro341Ala
XM_011527337.1:c.991C>G	XP_011525639.1:p.Pro331Ala
XM_011527338.1:c.991C>G	XP_011525640.1:p.Pro331Ala
NM_024876.4:c.991C>G MANE Select	NP_079152.3:p.Pro331Ala
NM_001142555.3:c.868C>G	NP_001136027.1:p.Pro290Ala