Canonical Allele Identifier: CA345054326

Gene: COQ8A

Linked Data

• gnomAD v4: 1-226983836-C-A
• MyVariant Identifiers: chr1:g.227171537C>A (hg19) ; chr1:g.226983836C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226983836C>A , CM000663.2:g.226983836C>A	GRCh38
NC_000001.10:g.227171537C>A , CM000663.1:g.227171537C>A	GRCh37
NC_000001.9:g.225238160C>A	NCBI36
NG_012825.1:g.48600C>A
NG_012825.2:g.91301C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.1238C>A MANE Select	ENSP00000355739.3:p.Ala413Asp
ENST00000366779.6:c.*5965C>A	ENSP00000355741.2:n.*5965C>A
ENST00000676884.1:c.*6087C>A	ENSP00000503200.1:n.*6087C>A
ENST00000366777.3:c.1238C>A	ENSP00000355739.3:p.Ala413Asp
ENST00000366778.5:c.1082C>A	ENSP00000355740.1:p.Ala361Asp
ENST00000366779.5:c.1238C>A	ENSP00000355741.1:p.Ala413Asp
ENST00000478406.5:n.1861C>A
ENST00000479852.1:n.186C>A
ENST00000485462.5:n.628C>A
NM_020247.4:c.1238C>A	NP_064632.2:p.Ala413Asp
XM_005273201.1:c.1238C>A	XP_005273258.1:p.Ala413Asp
XM_011544238.1:c.1238C>A	XP_011542540.1:p.Ala413Asp
XM_011544239.1:c.1238C>A	XP_011542541.1:p.Ala413Asp
XM_011544240.1:c.1238C>A	XP_011542542.1:p.Ala413Asp
XM_011544241.1:c.1238C>A	XP_011542543.1:p.Ala413Asp
XM_011544239.2:c.1238C>A	XP_011542541.1:p.Ala413Asp
XM_011544241.2:c.1238C>A	XP_011542543.1:p.Ala413Asp
XM_017001852.1:c.1238C>A	XP_016857341.1:p.Ala413Asp
XM_024448517.1:c.1238C>A	XP_024304285.1:p.Ala413Asp
XM_024448518.1:c.1238C>A	XP_024304286.1:p.Ala413Asp
NM_020247.5:c.1238C>A MANE Select	NP_064632.2:p.Ala413Asp