Canonical Allele Identifier: CA1880225374

Gene: COQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128323172_128323173delinsCG , CM000671.2:g.128323172_128323173delinsCG	GRCh38
NC_000009.11:g.131085451_131085452delinsCG , CM000671.1:g.131085451_131085452delinsCG	GRCh37
NC_000009.10:g.130125272_130125273delinsCG	NCBI36
NG_042101.1:g.5665_5666delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300452.8:c.202+25_202+26delinsCG MANE Select	ENSP00000300452.3:n.202+25_202+26delinsCG
ENST00000300452.7:c.202+25_202+26delinsCG	ENSP00000300452.3:n.202+25_202+26delinsCG
ENST00000372875.3:c.202+25_202+26delinsCG	ENSP00000361966.3:n.202+25_202+26delinsCG
ENST00000608951.5:c.202+25_202+26delinsCG	ENSP00000476323.1:n.202+25_202+26delinsCG
ENST00000609948.1:c.227_228delinsCG	ENSP00000477292.1:p.Pro76=
NM_001305942.1:c.202+25_202+26delinsCG	NP_001292871.1:n.202+25_202+26delinsCG
NM_016035.3:c.202+25_202+26delinsCG	NP_057119.2:n.202+25_202+26delinsCG
NM_016035.4:c.202+25_202+26delinsCG	NP_057119.2:n.202+25_202+26delinsCG
XM_011518761.1:c.202+25_202+26delinsCG	XP_011517063.1:n.202+25_202+26delinsCG
XR_929805.1:n.548+25_548+26delinsCG
XM_017014792.1:c.202+25_202+26delinsCG	XP_016870281.1:n.202+25_202+26delinsCG
XM_017014793.1:c.202+25_202+26delinsCG	XP_016870282.1:n.202+25_202+26delinsCG
XR_001746316.2:n.552+25_552+26delinsCG
XR_929805.3:n.548+25_548+26delinsCG
NM_016035.5:c.202+25_202+26delinsCG MANE Select	NP_057119.3:n.202+25_202+26delinsCG
NM_001305942.2:c.202+25_202+26delinsCG	NP_001292871.2:n.202+25_202+26delinsCG