Canonical Allele Identifier: CA467270745

Gene: COQ4

Linked Data

• MyVariant Identifiers: chr9:g.131085335A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128323056A>C , CM000671.2:g.128323056A>C	GRCh38
NC_000009.11:g.131085335A>C , CM000671.1:g.131085335A>C	GRCh37
NC_000009.10:g.130125156A>C	NCBI36
NG_042101.1:g.5549A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300452.8:c.111A>C MANE Select	ENSP00000300452.3:p.Leu37=
ENST00000300452.7:c.111A>C	ENSP00000300452.3:p.Leu37=
ENST00000372875.3:c.111A>C	ENSP00000361966.3:p.Leu37=
ENST00000608951.5:c.111A>C	ENSP00000476323.1:p.Leu37=
ENST00000609948.1:c.111A>C	ENSP00000477292.1:p.Leu37=
NM_001305942.1:c.111A>C	NP_001292871.1:p.Leu37=
NM_016035.3:c.111A>C	NP_057119.2:p.Leu37=
NM_016035.4:c.111A>C	NP_057119.2:p.Leu37=
XM_011518761.1:c.111A>C	XP_011517063.1:p.Leu37=
XR_929805.1:n.457A>C
XM_017014792.1:c.111A>C	XP_016870281.1:p.Leu37=
XM_017014793.1:c.111A>C	XP_016870282.1:p.Leu37=
XR_001746316.2:n.461A>C
XR_929805.3:n.457A>C
NM_016035.5:c.111A>C MANE Select	NP_057119.3:p.Leu37=
NM_001305942.2:c.111A>C	NP_001292871.2:p.Leu37=