Canonical Allele Identifier: CA1880227588

Gene: COQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128325835C= , CM000671.2:g.128325835C=	GRCh38
NC_000009.11:g.131088114C= , CM000671.1:g.131088114C=	GRCh37
NC_000009.10:g.130127935C=	NCBI36
NG_042101.1:g.8328C=

Transcript Alleles

HGVS	Amino-acid Change
NM_016035.5:c.356C= MANE Select	NP_057119.3:p.Pro119=
ENST00000300452.8:c.356C= MANE Select	ENSP00000300452.3:p.Pro119=
NM_001305942.1:c.259C=	NP_001292871.1:p.Arg87=
NM_001305942.2:c.259C=	NP_001292871.2:p.Arg87=
NM_016035.3:c.356C=	NP_057119.2:p.Pro119=
NM_016035.4:c.356C=	NP_057119.2:p.Pro119=
ENST00000300452.7:c.356C=	ENSP00000300452.3:p.Pro119=
ENST00000372875.3:c.356C=	ENSP00000361966.3:p.Pro119=
XM_011518761.1:c.356C=	XP_011517063.1:p.Pro119=
XM_017014792.1:c.259C=	XP_016870281.1:p.Arg87=
XM_017014793.1:c.259C=	XP_016870282.1:p.Arg87=
XR_001746316.2:n.609C=
XR_929805.1:n.702C=
XR_929805.3:n.702C=