Canonical Allele Identifier: CA423526795

Gene: COQ8A

Linked Data

• gnomAD v4: 1-226982956-G-A
• MyVariant Identifiers: chr1:g.227170657G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226982956G>A , CM000663.2:g.226982956G>A	GRCh38
NC_000001.10:g.227170657G>A , CM000663.1:g.227170657G>A	GRCh37
NC_000001.9:g.225237280G>A	NCBI36
NG_012825.1:g.47720G>A
NG_012825.2:g.90421G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.1002G>A MANE Select	ENSP00000355739.3:p.Arg334=
ENST00000366779.6:c.*5729G>A	ENSP00000355741.2:n.*5729G>A
ENST00000676884.1:c.*5851G>A	ENSP00000503200.1:n.*5851G>A
ENST00000366777.3:c.1002G>A	ENSP00000355739.3:p.Arg334=
ENST00000366778.5:c.846G>A	ENSP00000355740.1:p.Arg282=
ENST00000366779.5:c.1002G>A	ENSP00000355741.1:p.Arg334=
ENST00000478406.5:n.981G>A
ENST00000485462.5:n.392G>A
NM_020247.4:c.1002G>A	NP_064632.2:p.Arg334=
XM_005273201.1:c.1002G>A	XP_005273258.1:p.Arg334=
XM_011544238.1:c.1002G>A	XP_011542540.1:p.Arg334=
XM_011544239.1:c.1002G>A	XP_011542541.1:p.Arg334=
XM_011544240.1:c.1002G>A	XP_011542542.1:p.Arg334=
XM_011544241.1:c.1002G>A	XP_011542543.1:p.Arg334=
XM_011544239.2:c.1002G>A	XP_011542541.1:p.Arg334=
XM_011544241.2:c.1002G>A	XP_011542543.1:p.Arg334=
XM_017001852.1:c.1002G>A	XP_016857341.1:p.Arg334=
XM_024448517.1:c.1002G>A	XP_024304285.1:p.Arg334=
XM_024448518.1:c.1002G>A	XP_024304286.1:p.Arg334=
NM_020247.5:c.1002G>A MANE Select	NP_064632.2:p.Arg334=