Canonical Allele Identifier: CA1880225152

Gene: COQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128323031C= , CM000671.2:g.128323031C=	GRCh38
NC_000009.11:g.131085310C= , CM000671.1:g.131085310C=	GRCh37
NC_000009.10:g.130125131C=	NCBI36
NG_042101.1:g.5524C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300452.8:c.86C= MANE Select	ENSP00000300452.3:p.Ala29=
ENST00000300452.7:c.86C=	ENSP00000300452.3:p.Ala29=
ENST00000372875.3:c.86C=	ENSP00000361966.3:p.Ala29=
ENST00000608951.5:c.86C=	ENSP00000476323.1:p.Ala29=
ENST00000609948.1:c.86C=	ENSP00000477292.1:p.Ala29=
NM_001305942.1:c.86C=	NP_001292871.1:p.Ala29=
NM_016035.3:c.86C=	NP_057119.2:p.Ala29=
NM_016035.4:c.86C=	NP_057119.2:p.Ala29=
XM_011518761.1:c.86C=	XP_011517063.1:p.Ala29=
XR_929805.1:n.432C=
XM_017014792.1:c.86C=	XP_016870281.1:p.Ala29=
XM_017014793.1:c.86C=	XP_016870282.1:p.Ala29=
XR_001746316.2:n.436C=
XR_929805.3:n.432C=
NM_016035.5:c.86C= MANE Select	NP_057119.3:p.Ala29=
NM_001305942.2:c.86C=	NP_001292871.2:p.Ala29=