Canonical Allele Identifier: CA345052041

Gene: COQ8A

Linked Data

• MyVariant Identifiers: chr1:g.227169796C>G (hg19) ; chr1:g.226982095C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226982095C>G , CM000663.2:g.226982095C>G	GRCh38
NC_000001.10:g.227169796C>G , CM000663.1:g.227169796C>G	GRCh37
NC_000001.9:g.225236419C>G	NCBI36
NG_012825.1:g.46859C>G
NG_012825.2:g.89560C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.799C>G MANE Select	ENSP00000355739.3:p.Leu267Val
ENST00000366779.6:c.*5526C>G	ENSP00000355741.2:n.*5526C>G
ENST00000676884.1:c.*5648C>G	ENSP00000503200.1:n.*5648C>G
ENST00000366777.3:c.799C>G	ENSP00000355739.3:p.Leu267Val
ENST00000366778.5:c.643C>G	ENSP00000355740.1:p.Leu215Val
ENST00000366779.5:c.799C>G	ENSP00000355741.1:p.Leu267Val
ENST00000478406.5:n.250C>G
ENST00000485462.5:n.189C>G
NM_020247.4:c.799C>G	NP_064632.2:p.Leu267Val
XM_005273201.1:c.799C>G	XP_005273258.1:p.Leu267Val
XM_011544238.1:c.799C>G	XP_011542540.1:p.Leu267Val
XM_011544239.1:c.799C>G	XP_011542541.1:p.Leu267Val
XM_011544240.1:c.799C>G	XP_011542542.1:p.Leu267Val
XM_011544241.1:c.799C>G	XP_011542543.1:p.Leu267Val
XM_011544239.2:c.799C>G	XP_011542541.1:p.Leu267Val
XM_011544241.2:c.799C>G	XP_011542543.1:p.Leu267Val
XM_017001852.1:c.799C>G	XP_016857341.1:p.Leu267Val
XM_024448517.1:c.799C>G	XP_024304285.1:p.Leu267Val
XM_024448518.1:c.799C>G	XP_024304286.1:p.Leu267Val
NM_020247.5:c.799C>G MANE Select	NP_064632.2:p.Leu267Val