Canonical Allele Identifier: CA345052775

Gene: COQ8A

Linked Data

• gnomAD v4: 1-226982931-A-G
• MyVariant Identifiers: chr1:g.227170632A>G (hg19) ; chr1:g.226982931A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226982931A>G , CM000663.2:g.226982931A>G	GRCh38
NC_000001.10:g.227170632A>G , CM000663.1:g.227170632A>G	GRCh37
NC_000001.9:g.225237255A>G	NCBI36
NG_012825.1:g.47695A>G
NG_012825.2:g.90396A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.977A>G MANE Select	ENSP00000355739.3:p.Asp326Gly
ENST00000366779.6:c.*5704A>G	ENSP00000355741.2:n.*5704A>G
ENST00000676884.1:c.*5826A>G	ENSP00000503200.1:n.*5826A>G
ENST00000366777.3:c.977A>G	ENSP00000355739.3:p.Asp326Gly
ENST00000366778.5:c.821A>G	ENSP00000355740.1:p.Asp274Gly
ENST00000366779.5:c.977A>G	ENSP00000355741.1:p.Asp326Gly
ENST00000478406.5:n.956A>G
ENST00000485462.5:n.367A>G
NM_020247.4:c.977A>G	NP_064632.2:p.Asp326Gly
XM_005273201.1:c.977A>G	XP_005273258.1:p.Asp326Gly
XM_011544238.1:c.977A>G	XP_011542540.1:p.Asp326Gly
XM_011544239.1:c.977A>G	XP_011542541.1:p.Asp326Gly
XM_011544240.1:c.977A>G	XP_011542542.1:p.Asp326Gly
XM_011544241.1:c.977A>G	XP_011542543.1:p.Asp326Gly
XM_011544239.2:c.977A>G	XP_011542541.1:p.Asp326Gly
XM_011544241.2:c.977A>G	XP_011542543.1:p.Asp326Gly
XM_017001852.1:c.977A>G	XP_016857341.1:p.Asp326Gly
XM_024448517.1:c.977A>G	XP_024304285.1:p.Asp326Gly
XM_024448518.1:c.977A>G	XP_024304286.1:p.Asp326Gly
NM_020247.5:c.977A>G MANE Select	NP_064632.2:p.Asp326Gly