Canonical Allele Identifier: CA8076217

Gene: COQ9

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.57456592G>A , CM000678.2:g.57456592G>A	GRCh38
NC_000016.9:g.57490504G>A , CM000678.1:g.57490504G>A	GRCh37
NC_000016.8:g.56048005G>A	NCBI36
NG_027696.1:g.14168G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262507.11:c.467G>A MANE Select	ENSP00000262507.5:p.Arg156Gln
ENST00000262507.10:c.467G>A	ENSP00000262507.5:p.Arg156Gln
ENST00000562426.5:n.470G>A
ENST00000562734.5:n.491G>A
ENST00000563166.1:c.303+3677G>A	ENSP00000455495.1:n.303+3677G>A
ENST00000563391.1:c.59G>A	ENSP00000455516.1:p.Arg20Gln
ENST00000564115.5:c.467G>A	ENSP00000455256.1:p.Arg156Gln
ENST00000564655.5:c.479G>A	ENSP00000454992.1:p.Arg160Gln
ENST00000565964.5:c.379-1654G>A	ENSP00000458023.1:n.379-1654G>A
ENST00000567072.5:c.467G>A	ENSP00000456728.1:p.Arg156Gln
ENST00000567480.1:n.407G>A
ENST00000567576.1:n.190G>A
ENST00000567933.5:c.379-2973G>A	ENSP00000456174.1:n.379-2973G>A
ENST00000568790.5:n.491G>A
NM_020312.3:c.467G>A	NP_064708.1:p.Arg156Gln
NM_020312.4:c.467G>A MANE Select	NP_064708.1:p.Arg156Gln