Canonical Allele Identifier: CA375017502
Gene: COQ4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128323108G>A , CM000671.2:g.128323108G>A GRCh38
NC_000009.11:g.131085387G>A , CM000671.1:g.131085387G>A GRCh37
NC_000009.10:g.130125208G>A NCBI36
NG_042101.1:g.5601G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300452.8:c.163G>A MANE Select ENSP00000300452.3:p.Gly55Ser
ENST00000300452.7:c.163G>A ENSP00000300452.3:p.Gly55Ser
ENST00000372875.3:c.163G>A ENSP00000361966.3:p.Gly55Ser
ENST00000608951.5:c.163G>A ENSP00000476323.1:p.Gly55Ser
ENST00000609948.1:c.163G>A ENSP00000477292.1:p.Gly55Ser
NM_001305942.1:c.163G>A NP_001292871.1:p.Gly55Ser
NM_016035.3:c.163G>A NP_057119.2:p.Gly55Ser
NM_016035.4:c.163G>A NP_057119.2:p.Gly55Ser
XM_011518761.1:c.163G>A XP_011517063.1:p.Gly55Ser
XR_929805.1:n.509G>A
XM_017014792.1:c.163G>A XP_016870281.1:p.Gly55Ser
XM_017014793.1:c.163G>A XP_016870282.1:p.Gly55Ser
XR_001746316.2:n.513G>A
XR_929805.3:n.509G>A
NM_016035.5:c.163G>A MANE Select NP_057119.3:p.Gly55Ser
NM_001305942.2:c.163G>A NP_001292871.2:p.Gly55Ser