Canonical Allele Identifier: CA5260570
Gene: COQ4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128332171C>A , CM000671.2:g.128332171C>A GRCh38
NC_000009.11:g.131094450C>A , CM000671.1:g.131094450C>A GRCh37
NC_000009.10:g.130134271C>A NCBI36
NG_042101.1:g.14664C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300452.8:c.421C>A MANE Select ENSP00000300452.3:p.Arg141=
ENST00000300452.7:c.421C>A ENSP00000300452.3:p.Arg141=
ENST00000461102.1:n.1760C>A
NM_001305942.1:c.*3-1303C>A NP_001292871.1:n.*3-1303C>A
NM_016035.3:c.421C>A NP_057119.2:p.Arg141=
NM_016035.4:c.421C>A NP_057119.2:p.Arg141=
XR_929805.1:n.749-679C>A
XM_017014792.1:c.*3-679C>A XP_016870281.1:n.*3-679C>A
XR_001746316.2:n.674C>A
XR_929805.3:n.749-679C>A
NM_016035.5:c.421C>A MANE Select NP_057119.3:p.Arg141=
NM_001305942.2:c.*3-1303C>A NP_001292871.2:n.*3-1303C>A