Canonical Allele Identifier: CA1472713129

Gene: COQ2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.83279200_83279204delinsTAAAG , CM000666.2:g.83279200_83279204delinsTAAAG	GRCh38
NC_000004.11:g.84200353_84200357delinsTAAAG , CM000666.1:g.84200353_84200357delinsTAAAG	GRCh37
NC_000004.10:g.84419377_84419381delinsTAAAG	NCBI36
NG_015825.1:g.10711_10715delinsCTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311469.9:c.404-90_404-86delinsCTTTA	ENSP00000310873.4:n.404-90_404-86delinsCTTTA
ENST00000647002.2:c.254-90_254-86delinsCTTTA MANE Select	ENSP00000495761.2:n.254-90_254-86delinsCTTTA
ENST00000311461.7:c.254-90_254-86delinsCTTTA	ENSP00000311835.7:n.254-90_254-86delinsCTTTA
ENST00000311469.8:c.404-90_404-86delinsCTTTA	ENSP00000310873.4:n.404-90_404-86delinsCTTTA
ENST00000503391.5:c.254-90_254-86delinsCTTTA	ENSP00000426242.1:n.254-90_254-86delinsCTTTA
ENST00000514935.1:n.166-90_166-86delinsCTTTA
NM_015697.7:c.404-90_404-86delinsCTTTA	NP_056512.5:n.404-90_404-86delinsCTTTA
XM_011531855.1:c.404-90_404-86delinsCTTTA	XP_011530157.1:n.404-90_404-86delinsCTTTA
XM_011531856.1:c.404-90_404-86delinsCTTTA	XP_011530158.1:n.404-90_404-86delinsCTTTA
XM_011531857.1:c.404-90_404-86delinsCTTTA	XP_011530159.1:n.404-90_404-86delinsCTTTA
XM_011531858.1:c.404-90_404-86delinsCTTTA	XP_011530160.1:n.404-90_404-86delinsCTTTA
XM_011531859.1:c.404-90_404-86delinsCTTTA	XP_011530161.1:n.404-90_404-86delinsCTTTA
XM_011531860.1:c.404-90_404-86delinsCTTTA	XP_011530162.1:n.404-90_404-86delinsCTTTA
XM_011531861.1:c.404-90_404-86delinsCTTTA	XP_011530163.1:n.404-90_404-86delinsCTTTA
XM_011531862.1:c.404-90_404-86delinsCTTTA	XP_011530164.1:n.404-90_404-86delinsCTTTA
XM_011531863.1:c.404-90_404-86delinsCTTTA	XP_011530165.1:n.404-90_404-86delinsCTTTA
XM_011531864.1:c.404-90_404-86delinsCTTTA	XP_011530166.1:n.404-90_404-86delinsCTTTA
XM_011531865.1:c.404-90_404-86delinsCTTTA	XP_011530167.1:n.404-90_404-86delinsCTTTA
XM_011531866.1:c.404-90_404-86delinsCTTTA	XP_011530168.1:n.404-90_404-86delinsCTTTA
XM_011531867.1:c.50-90_50-86delinsCTTTA	XP_011530169.1:n.50-90_50-86delinsCTTTA
XR_427543.2:n.563-90_563-86delinsCTTTA
XR_938721.1:n.579-90_579-86delinsCTTTA
NM_001358921.1:c.254-90_254-86delinsCTTTA	NP_001345850.1:n.254-90_254-86delinsCTTTA
NM_015697.8:c.404-90_404-86delinsCTTTA	NP_056512.5:n.404-90_404-86delinsCTTTA
XM_011531855.3:c.254-90_254-86delinsCTTTA	XP_011530157.2:n.254-90_254-86delinsCTTTA
XM_011531857.3:c.254-90_254-86delinsCTTTA	XP_011530159.2:n.254-90_254-86delinsCTTTA
XM_011531859.3:c.254-90_254-86delinsCTTTA	XP_011530161.2:n.254-90_254-86delinsCTTTA
XM_011531860.3:c.254-90_254-86delinsCTTTA	XP_011530162.2:n.254-90_254-86delinsCTTTA
XM_011531862.3:c.254-90_254-86delinsCTTTA	XP_011530164.2:n.254-90_254-86delinsCTTTA
XM_011531863.3:c.254-90_254-86delinsCTTTA	XP_011530165.2:n.254-90_254-86delinsCTTTA
XM_011531866.3:c.254-90_254-86delinsCTTTA	XP_011530168.2:n.254-90_254-86delinsCTTTA
XM_011531867.3:c.50-90_50-86delinsCTTTA	XP_011530169.1:n.50-90_50-86delinsCTTTA
XM_017008031.2:c.50-90_50-86delinsCTTTA	XP_016863520.1:n.50-90_50-86delinsCTTTA
XR_001741203.2:n.285-90_285-86delinsCTTTA
XR_001741204.2:n.285-90_285-86delinsCTTTA
XR_427543.4:n.285-90_285-86delinsCTTTA
XR_938721.3:n.285-90_285-86delinsCTTTA
NM_001358921.2:c.254-90_254-86delinsCTTTA MANE Select	NP_001345850.1:n.254-90_254-86delinsCTTTA
NM_015697.9:c.404-90_404-86delinsCTTTA	NP_056512.5:n.404-90_404-86delinsCTTTA