Canonical Allele Identifier: CA8076156

Gene: COQ9

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.57452900C>T , CM000678.2:g.57452900C>T	GRCh38
NC_000016.9:g.57486812C>T , CM000678.1:g.57486812C>T	GRCh37
NC_000016.8:g.56044313C>T	NCBI36
NG_027696.1:g.10476C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262507.11:c.342C>T MANE Select	ENSP00000262507.5:p.His114=
ENST00000262507.10:c.342C>T	ENSP00000262507.5:p.His114=
ENST00000562426.5:n.345C>T
ENST00000562734.5:n.366C>T
ENST00000563166.1:c.288C>T	ENSP00000455495.1:p.His96=
ENST00000563391.1:c.-67C>T	ENSP00000455516.1:n.-67C>T
ENST00000564115.5:c.342C>T	ENSP00000455256.1:p.His114=
ENST00000564655.5:c.354C>T	ENSP00000454992.1:p.His118=
ENST00000565964.5:c.342C>T	ENSP00000458023.1:p.His114=
ENST00000566388.5:n.423C>T
ENST00000567072.5:c.342C>T	ENSP00000456728.1:p.His114=
ENST00000567480.1:n.272C>T
ENST00000567933.5:c.342C>T	ENSP00000456174.1:p.His114=
ENST00000568790.5:n.366C>T
NM_020312.3:c.342C>T	NP_064708.1:p.His114=
NM_020312.4:c.342C>T MANE Select	NP_064708.1:p.His114=