Canonical Allele Identifier: CA289302

Gene: COQ8A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226965080A>C , CM000663.2:g.226965080A>C	GRCh38
NC_000001.10:g.227152781A>C , CM000663.1:g.227152781A>C	GRCh37
NC_000001.9:g.225219404A>C	NCBI36
NG_012825.1:g.29844A>C
NG_012825.2:g.72545A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.258A>C MANE Select	ENSP00000355739.3:p.Ala86=
ENST00000366779.6:c.*4985A>C	ENSP00000355741.2:n.*4985A>C
ENST00000676884.1:c.*5107A>C	ENSP00000503200.1:n.*5107A>C
ENST00000366777.3:c.258A>C	ENSP00000355739.3:p.Ala86=
ENST00000366778.5:c.102A>C	ENSP00000355740.1:p.Ala34=
ENST00000366779.5:c.258A>C	ENSP00000355741.1:p.Ala86=
ENST00000478406.5:n.107-12369A>C
ENST00000489044.1:n.469A>C
NM_020247.4:c.258A>C	NP_064632.2:p.Ala86=
XM_005273201.1:c.258A>C	XP_005273258.1:p.Ala86=
XM_011544238.1:c.258A>C	XP_011542540.1:p.Ala86=
XM_011544239.1:c.258A>C	XP_011542541.1:p.Ala86=
XM_011544240.1:c.258A>C	XP_011542542.1:p.Ala86=
XM_011544241.1:c.258A>C	XP_011542543.1:p.Ala86=
XM_011544239.2:c.258A>C	XP_011542541.1:p.Ala86=
XM_011544241.2:c.258A>C	XP_011542543.1:p.Ala86=
XM_017001852.1:c.258A>C	XP_016857341.1:p.Ala86=
XM_024448517.1:c.258A>C	XP_024304285.1:p.Ala86=
XM_024448518.1:c.258A>C	XP_024304286.1:p.Ala86=
NM_020247.5:c.258A>C MANE Select	NP_064632.2:p.Ala86=