Canonical Allele Identifier: CA2671245771

Gene: COQ2

Linked Data

• gnomAD v4: 4-83279126-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.83279130_83279131del , CM000666.2:g.83279130_83279131del	GRCh38
NC_000004.11:g.84200283_84200284del , CM000666.1:g.84200283_84200284del	GRCh37
NC_000004.10:g.84419307_84419308del	NCBI36
NG_015825.1:g.10787_10788del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311469.9:c.404-14_404-13del	ENSP00000310873.4:n.404-14_404-13del
ENST00000647002.2:c.254-14_254-13del MANE Select	ENSP00000495761.2:n.254-14_254-13del
ENST00000311461.7:c.254-14_254-13del	ENSP00000311835.7:n.254-14_254-13del
ENST00000311469.8:c.404-14_404-13del	ENSP00000310873.4:n.404-14_404-13del
ENST00000503391.5:c.254-14_254-13del	ENSP00000426242.1:n.254-14_254-13del
ENST00000514935.1:n.166-14_166-13del
NM_015697.7:c.404-14_404-13del	NP_056512.5:n.404-14_404-13del
XM_011531855.1:c.404-14_404-13del	XP_011530157.1:n.404-14_404-13del
XM_011531856.1:c.404-14_404-13del	XP_011530158.1:n.404-14_404-13del
XM_011531857.1:c.404-14_404-13del	XP_011530159.1:n.404-14_404-13del
XM_011531858.1:c.404-14_404-13del	XP_011530160.1:n.404-14_404-13del
XM_011531859.1:c.404-14_404-13del	XP_011530161.1:n.404-14_404-13del
XM_011531860.1:c.404-14_404-13del	XP_011530162.1:n.404-14_404-13del
XM_011531861.1:c.404-14_404-13del	XP_011530163.1:n.404-14_404-13del
XM_011531862.1:c.404-14_404-13del	XP_011530164.1:n.404-14_404-13del
XM_011531863.1:c.404-14_404-13del	XP_011530165.1:n.404-14_404-13del
XM_011531864.1:c.404-14_404-13del	XP_011530166.1:n.404-14_404-13del
XM_011531865.1:c.404-14_404-13del	XP_011530167.1:n.404-14_404-13del
XM_011531866.1:c.404-14_404-13del	XP_011530168.1:n.404-14_404-13del
XM_011531867.1:c.50-14_50-13del	XP_011530169.1:n.50-14_50-13del
XR_427543.2:n.563-14_563-13del
XR_938721.1:n.579-14_579-13del
NM_001358921.1:c.254-14_254-13del	NP_001345850.1:n.254-14_254-13del
NM_015697.8:c.404-14_404-13del	NP_056512.5:n.404-14_404-13del
XM_011531855.3:c.254-14_254-13del	XP_011530157.2:n.254-14_254-13del
XM_011531857.3:c.254-14_254-13del	XP_011530159.2:n.254-14_254-13del
XM_011531859.3:c.254-14_254-13del	XP_011530161.2:n.254-14_254-13del
XM_011531860.3:c.254-14_254-13del	XP_011530162.2:n.254-14_254-13del
XM_011531862.3:c.254-14_254-13del	XP_011530164.2:n.254-14_254-13del
XM_011531863.3:c.254-14_254-13del	XP_011530165.2:n.254-14_254-13del
XM_011531866.3:c.254-14_254-13del	XP_011530168.2:n.254-14_254-13del
XM_011531867.3:c.50-14_50-13del	XP_011530169.1:n.50-14_50-13del
XM_017008031.2:c.50-14_50-13del	XP_016863520.1:n.50-14_50-13del
XR_001741203.2:n.285-14_285-13del
XR_001741204.2:n.285-14_285-13del
XR_427543.4:n.285-14_285-13del
XR_938721.3:n.285-14_285-13del
NM_001358921.2:c.254-14_254-13del MANE Select	NP_001345850.1:n.254-14_254-13del
NM_015697.9:c.404-14_404-13del	NP_056512.5:n.404-14_404-13del