Canonical Allele Identifier: CA1880225188

Gene: COQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128323060T= , CM000671.2:g.128323060T=	GRCh38
NC_000009.11:g.131085339T= , CM000671.1:g.131085339T=	GRCh37
NC_000009.10:g.130125160T=	NCBI36
NG_042101.1:g.5553T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300452.8:c.115T= MANE Select	ENSP00000300452.3:p.Ser39=
ENST00000300452.7:c.115T=	ENSP00000300452.3:p.Ser39=
ENST00000372875.3:c.115T=	ENSP00000361966.3:p.Ser39=
ENST00000608951.5:c.115T=	ENSP00000476323.1:p.Ser39=
ENST00000609948.1:c.115T=	ENSP00000477292.1:p.Ser39=
NM_001305942.1:c.115T=	NP_001292871.1:p.Ser39=
NM_016035.3:c.115T=	NP_057119.2:p.Ser39=
NM_016035.4:c.115T=	NP_057119.2:p.Ser39=
XM_011518761.1:c.115T=	XP_011517063.1:p.Ser39=
XR_929805.1:n.461T=
XM_017014792.1:c.115T=	XP_016870281.1:p.Ser39=
XM_017014793.1:c.115T=	XP_016870282.1:p.Ser39=
XR_001746316.2:n.465T=
XR_929805.3:n.461T=
NM_016035.5:c.115T= MANE Select	NP_057119.3:p.Ser39=
NM_001305942.2:c.115T=	NP_001292871.2:p.Ser39=