Canonical Allele Identifier: CA345055726

Gene: COQ8A

Linked Data

• MyVariant Identifiers: chr1:g.227172313A>T (hg19) ; chr1:g.226984612A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226984612A>T , CM000663.2:g.226984612A>T	GRCh38
NC_000001.10:g.227172313A>T , CM000663.1:g.227172313A>T	GRCh37
NC_000001.9:g.225238936A>T	NCBI36
NG_012825.1:g.49376A>T
NG_012825.2:g.92077A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.1463A>T MANE Select	ENSP00000355739.3:p.Asp488Val
ENST00000366779.6:c.*6190A>T	ENSP00000355741.2:n.*6190A>T
ENST00000366777.3:c.1463A>T	ENSP00000355739.3:p.Asp488Val
ENST00000366778.5:c.1307A>T	ENSP00000355740.1:p.Asp436Val
ENST00000366779.5:c.1463A>T	ENSP00000355741.1:p.Asp488Val
ENST00000478406.5:n.2325A>T
ENST00000479852.1:n.650A>T
ENST00000485462.5:n.853A>T
NM_020247.4:c.1463A>T	NP_064632.2:p.Asp488Val
XM_005273201.1:c.1463A>T	XP_005273258.1:p.Asp488Val
XM_011544238.1:c.1463A>T	XP_011542540.1:p.Asp488Val
XM_011544239.1:c.1463A>T	XP_011542541.1:p.Asp488Val
XM_011544240.1:c.1463A>T	XP_011542542.1:p.Asp488Val
XM_011544241.1:c.1463A>T	XP_011542543.1:p.Asp488Val
XM_011544239.2:c.1463A>T	XP_011542541.1:p.Asp488Val
XM_011544241.2:c.1463A>T	XP_011542543.1:p.Asp488Val
XM_017001852.1:c.1463A>T	XP_016857341.1:p.Asp488Val
XM_024448517.1:c.1463A>T	XP_024304285.1:p.Asp488Val
XM_024448518.1:c.1463A>T	XP_024304286.1:p.Asp488Val
NM_020247.5:c.1463A>T MANE Select	NP_064632.2:p.Asp488Val