Canonical Allele Identifier: CA323351

Gene: COQ9

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.57451045C>G , CM000678.2:g.57451045C>G	GRCh38
NC_000016.9:g.57484957C>G , CM000678.1:g.57484957C>G	GRCh37
NC_000016.8:g.56042458C>G	NCBI36
NG_027696.1:g.8621C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262507.11:c.79C>G MANE Select	ENSP00000262507.5:p.Arg27Gly
ENST00000262507.10:c.79C>G	ENSP00000262507.5:p.Arg27Gly
ENST00000562426.5:n.82C>G
ENST00000562734.5:n.103C>G
ENST00000563166.1:c.25C>G	ENSP00000455495.1:p.Arg9Gly
ENST00000563391.1:c.-330C>G	ENSP00000455516.1:n.-330C>G
ENST00000564115.5:c.79C>G	ENSP00000455256.1:p.Arg27Gly
ENST00000564655.5:c.91C>G	ENSP00000454992.1:p.Arg31Gly
ENST00000565964.5:c.79C>G	ENSP00000458023.1:p.Arg27Gly
ENST00000566388.5:n.160C>G
ENST00000567072.5:c.79C>G	ENSP00000456728.1:p.Arg27Gly
ENST00000567384.1:n.261C>G
ENST00000567480.1:n.9C>G
ENST00000567933.5:c.79C>G	ENSP00000456174.1:p.Arg27Gly
ENST00000568790.5:n.103C>G
NM_020312.3:c.79C>G	NP_064708.1:p.Arg27Gly
NM_020312.4:c.79C>G MANE Select	NP_064708.1:p.Arg27Gly