Canonical Allele Identifier: CA8076155

Gene: COQ9

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.57452895G>A , CM000678.2:g.57452895G>A	GRCh38
NC_000016.9:g.57486807G>A , CM000678.1:g.57486807G>A	GRCh37
NC_000016.8:g.56044308G>A	NCBI36
NG_027696.1:g.10471G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262507.11:c.337G>A MANE Select	ENSP00000262507.5:p.Ala113Thr
ENST00000262507.10:c.337G>A	ENSP00000262507.5:p.Ala113Thr
ENST00000562426.5:n.340G>A
ENST00000562734.5:n.361G>A
ENST00000563166.1:c.283G>A	ENSP00000455495.1:p.Ala95Thr
ENST00000563391.1:c.-72G>A	ENSP00000455516.1:n.-72G>A
ENST00000564115.5:c.337G>A	ENSP00000455256.1:p.Ala113Thr
ENST00000564655.5:c.349G>A	ENSP00000454992.1:p.Ala117Thr
ENST00000565964.5:c.337G>A	ENSP00000458023.1:p.Ala113Thr
ENST00000566388.5:n.418G>A
ENST00000567072.5:c.337G>A	ENSP00000456728.1:p.Ala113Thr
ENST00000567480.1:n.267G>A
ENST00000567933.5:c.337G>A	ENSP00000456174.1:p.Ala113Thr
ENST00000568790.5:n.361G>A
NM_020312.3:c.337G>A	NP_064708.1:p.Ala113Thr
NM_020312.4:c.337G>A MANE Select	NP_064708.1:p.Ala113Thr