Canonical Allele Identifier: CA405957423

Gene: COQ8B

Linked Data

• MyVariant Identifiers: chr19:g.41198032T>A (hg19) ; chr19:g.40692127T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40692127T>A , CM000681.2:g.40692127T>A	GRCh38
NC_000019.9:g.41198032T>A , CM000681.1:g.41198032T>A	GRCh37
NC_000019.8:g.45889872T>A	NCBI36
NG_027800.1:g.29759A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324464.8:c.1543A>T MANE Select	ENSP00000315118.3:p.Thr515Ser
ENST00000593724.2:n.3366A>T
ENST00000594490.6:c.1465A>T	ENSP00000471310.2:p.Thr489Ser
ENST00000594720.6:c.1543A>T	ENSP00000470876.2:p.Thr515Ser
ENST00000596455.6:n.1835A>T
ENST00000601967.6:c.1543A>T	ENSP00000470916.2:p.Thr515Ser
ENST00000676555.1:c.*968A>T	ENSP00000503387.1:n.*968A>T
ENST00000676578.1:c.*1285A>T	ENSP00000504076.1:n.*1285A>T
ENST00000676960.1:n.1668A>T
ENST00000676962.1:n.1822A>T
ENST00000677018.1:c.1543A>T	ENSP00000503480.1:p.Thr515Ser
ENST00000677039.1:n.3746A>T
ENST00000677399.1:n.1985A>T
ENST00000677496.1:c.1216A>T	ENSP00000504773.1:p.Thr406Ser
ENST00000677517.1:c.1216A>T	ENSP00000503519.1:p.Thr406Ser
ENST00000677633.1:c.*966A>T	ENSP00000503645.1:n.*966A>T
ENST00000677800.1:c.*4647A>T	ENSP00000503794.1:n.*4647A>T
ENST00000678057.1:c.*1107A>T	ENSP00000503762.1:n.*1107A>T
ENST00000678119.1:n.1737A>T
ENST00000678166.1:n.1686A>T
ENST00000678312.1:n.1880A>T
ENST00000678316.1:c.*966A>T	ENSP00000504112.1:n.*966A>T
ENST00000678371.1:n.1993A>T
ENST00000678404.1:c.1543A>T	ENSP00000503944.1:p.Thr515Ser
ENST00000678419.1:c.1543A>T	ENSP00000504085.1:p.Thr515Ser
ENST00000678433.1:n.1899A>T
ENST00000678467.1:c.1543A>T	ENSP00000504072.1:p.Thr515Ser
ENST00000678569.1:c.*528A>T	ENSP00000504261.1:n.*528A>T
ENST00000678961.1:n.1898A>T
ENST00000679002.1:n.1722A>T
ENST00000679012.1:c.1099A>T	ENSP00000504446.1:p.Thr367Ser
ENST00000679070.1:c.*962A>T	ENSP00000503759.1:n.*962A>T
ENST00000679130.1:c.1543A>T	ENSP00000504845.1:p.Thr515Ser
ENST00000679315.1:c.*1373A>T	ENSP00000503065.1:n.*1373A>T
ENST00000243583.10:c.1420A>T	ENSP00000243583.5:p.Thr474Ser
ENST00000324464.7:c.1543A>T	ENSP00000315118.3:p.Thr515Ser
ENST00000593724.1:n.1658A>T
NM_001142555.2:c.1420A>T	NP_001136027.1:p.Thr474Ser
NM_024876.3:c.1543A>T	NP_079152.3:p.Thr515Ser
XM_005259270.3:c.1705A>T	XP_005259327.2:p.Thr569Ser
XM_005259271.3:c.1543A>T	XP_005259328.1:p.Thr515Ser
XM_005259272.3:c.1543A>T	XP_005259329.1:p.Thr515Ser
XM_005259273.3:c.1543A>T	XP_005259330.1:p.Thr515Ser
XM_006723392.2:c.1543A>T	XP_006723455.1:p.Thr515Ser
XM_006723393.2:c.1543A>T	XP_006723456.1:p.Thr515Ser
XM_011527334.1:c.1543A>T	XP_011525636.1:p.Thr515Ser
XM_011527335.1:c.1402A>T	XP_011525637.1:p.Thr468Ser
XM_011527336.1:c.1573A>T	XP_011525638.1:p.Thr525Ser
XM_011527337.1:c.1543A>T	XP_011525639.1:p.Thr515Ser
XM_011527338.1:c.1543A>T	XP_011525640.1:p.Thr515Ser
NM_024876.4:c.1543A>T MANE Select	NP_079152.3:p.Thr515Ser
NM_001142555.3:c.1420A>T	NP_001136027.1:p.Thr474Ser