Canonical Allele Identifier: CA5260475

Gene: COQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128325202C>G , CM000671.2:g.128325202C>G	GRCh38
NC_000009.11:g.131087481C>G , CM000671.1:g.131087481C>G	GRCh37
NC_000009.10:g.130127302C>G	NCBI36
NG_042101.1:g.7695C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300452.8:c.262C>G MANE Select	ENSP00000300452.3:p.Gln88Glu
ENST00000300452.7:c.262C>G	ENSP00000300452.3:p.Gln88Glu
ENST00000372875.3:c.262C>G	ENSP00000361966.3:p.Gln88Glu
NM_001305942.1:c.203-577C>G	NP_001292871.1:n.203-577C>G
NM_016035.3:c.262C>G	NP_057119.2:p.Gln88Glu
NM_016035.4:c.262C>G	NP_057119.2:p.Gln88Glu
XM_011518761.1:c.262C>G	XP_011517063.1:p.Gln88Glu
XR_929805.1:n.608C>G
XM_017014792.1:c.203-577C>G	XP_016870281.1:n.203-577C>G
XM_017014793.1:c.203-577C>G	XP_016870282.1:n.203-577C>G
XR_001746316.2:n.553-577C>G
XR_929805.3:n.608C>G
NM_016035.5:c.262C>G MANE Select	NP_057119.3:p.Gln88Glu
NM_001305942.2:c.203-577C>G	NP_001292871.2:n.203-577C>G