Canonical Allele Identifier: CA405963909

Gene: COQ8B

Linked Data

• MyVariant Identifiers: chr19:g.41209647G>T (hg19) ; chr19:g.40703742G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40703742G>T , CM000681.2:g.40703742G>T	GRCh38
NC_000019.9:g.41209647G>T , CM000681.1:g.41209647G>T	GRCh37
NC_000019.8:g.45901487G>T	NCBI36
NG_027800.1:g.18144C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.690C>A MANE Select	ENSP00000315118.3:p.Asp230Glu
ENST00000593724.2:n.393-120C>A
ENST00000594490.6:c.612C>A	ENSP00000471310.2:p.Asp204Glu
ENST00000594720.6:c.690C>A	ENSP00000470876.2:p.Asp230Glu
ENST00000596455.6:n.982C>A
ENST00000601967.6:c.690C>A	ENSP00000470916.2:p.Asp230Glu
ENST00000676555.1:c.690C>A	ENSP00000503387.1:p.Asp230Glu
ENST00000676578.1:c.*432C>A	ENSP00000504076.1:n.*432C>A
ENST00000676960.1:n.815C>A
ENST00000676962.1:n.969C>A
ENST00000677018.1:c.690C>A	ENSP00000503480.1:p.Asp230Glu
ENST00000677039.1:n.745C>A
ENST00000677399.1:n.1132C>A
ENST00000677496.1:c.363C>A	ENSP00000504773.1:p.Asp121Glu
ENST00000677517.1:c.363C>A	ENSP00000503519.1:p.Asp121Glu
ENST00000677633.1:c.*113C>A	ENSP00000503645.1:n.*113C>A
ENST00000677800.1:c.*3794C>A	ENSP00000503794.1:n.*3794C>A
ENST00000678057.1:c.*254C>A	ENSP00000503762.1:n.*254C>A
ENST00000678119.1:n.884C>A
ENST00000678166.1:n.861-120C>A
ENST00000678312.1:n.1027C>A
ENST00000678316.1:c.*113C>A	ENSP00000504112.1:n.*113C>A
ENST00000678371.1:n.1048C>A
ENST00000678404.1:c.690C>A	ENSP00000503944.1:p.Asp230Glu
ENST00000678419.1:c.690C>A	ENSP00000504085.1:p.Asp230Glu
ENST00000678433.1:n.1050C>A
ENST00000678467.1:c.690C>A	ENSP00000504072.1:p.Asp230Glu
ENST00000678569.1:c.690C>A	ENSP00000504261.1:p.Asp230Glu
ENST00000678961.1:n.873C>A
ENST00000679002.1:n.869C>A
ENST00000679012.1:c.246C>A	ENSP00000504446.1:p.Asp82Glu
ENST00000679070.1:c.*113C>A	ENSP00000503759.1:n.*113C>A
ENST00000679130.1:c.690C>A	ENSP00000504845.1:p.Asp230Glu
ENST00000679315.1:c.*520C>A	ENSP00000503065.1:n.*520C>A
ENST00000243583.10:c.567C>A	ENSP00000243583.5:p.Asp189Glu
ENST00000324464.7:c.690C>A	ENSP00000315118.3:p.Asp230Glu
ENST00000595254.5:c.363C>A	ENSP00000470894.1:p.Asp121Glu
ENST00000596455.5:n.810C>A
ENST00000599643.5:c.336-120C>A	ENSP00000471192.1:n.336-120C>A
ENST00000601304.5:c.*464C>A	ENSP00000472519.1:n.*464C>A
ENST00000601967.5:c.690C>A	ENSP00000470916.1:p.Asp230Glu
NM_001142555.2:c.567C>A	NP_001136027.1:p.Asp189Glu
NM_024876.3:c.690C>A	NP_079152.3:p.Asp230Glu
XM_005259270.3:c.852C>A	XP_005259327.2:p.Asp284Glu
XM_005259271.3:c.690C>A	XP_005259328.1:p.Asp230Glu
XM_005259272.3:c.690C>A	XP_005259329.1:p.Asp230Glu
XM_005259273.3:c.690C>A	XP_005259330.1:p.Asp230Glu
XM_006723392.2:c.690C>A	XP_006723455.1:p.Asp230Glu
XM_006723393.2:c.690C>A	XP_006723456.1:p.Asp230Glu
XM_011527334.1:c.690C>A	XP_011525636.1:p.Asp230Glu
XM_011527335.1:c.577-120C>A	XP_011525637.1:n.577-120C>A
XM_011527336.1:c.720C>A	XP_011525638.1:p.Asp240Glu
XM_011527337.1:c.690C>A	XP_011525639.1:p.Asp230Glu
XM_011527338.1:c.690C>A	XP_011525640.1:p.Asp230Glu
NM_024876.4:c.690C>A MANE Select	NP_079152.3:p.Asp230Glu
NM_001142555.3:c.567C>A	NP_001136027.1:p.Asp189Glu