Canonical Allele Identifier: CA151595

Gene: COQ8A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226961502G>A , CM000663.2:g.226961502G>A	GRCh38
NC_000001.10:g.227149203G>A , CM000663.1:g.227149203G>A	GRCh37
NC_000001.9:g.225215826G>A	NCBI36
NG_012825.1:g.26266G>A
NG_012825.2:g.68967G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.117G>A MANE Select	ENSP00000355739.3:p.Ala39=
ENST00000366779.6:c.*4844G>A	ENSP00000355741.2:n.*4844G>A
ENST00000676884.1:c.*4966G>A	ENSP00000503200.1:n.*4966G>A
ENST00000366777.3:c.117G>A	ENSP00000355739.3:p.Ala39=
ENST00000366778.5:c.-34-6G>A	ENSP00000355740.1:n.-34-6G>A
ENST00000366779.5:c.117G>A	ENSP00000355741.1:p.Ala39=
ENST00000478406.5:n.107-15947G>A
ENST00000489044.1:n.328G>A
NM_020247.4:c.117G>A	NP_064632.2:p.Ala39=
XM_005273201.1:c.117G>A	XP_005273258.1:p.Ala39=
XM_011544238.1:c.117G>A	XP_011542540.1:p.Ala39=
XM_011544239.1:c.117G>A	XP_011542541.1:p.Ala39=
XM_011544240.1:c.117G>A	XP_011542542.1:p.Ala39=
XM_011544241.1:c.117G>A	XP_011542543.1:p.Ala39=
XM_011544239.2:c.117G>A	XP_011542541.1:p.Ala39=
XM_011544241.2:c.117G>A	XP_011542543.1:p.Ala39=
XM_017001852.1:c.117G>A	XP_016857341.1:p.Ala39=
XM_024448517.1:c.117G>A	XP_024304285.1:p.Ala39=
XM_024448518.1:c.117G>A	XP_024304286.1:p.Ala39=
NM_020247.5:c.117G>A MANE Select	NP_064632.2:p.Ala39=