Canonical Allele Identifier: CA357230571

Gene: COQ2

Linked Data

• MyVariant Identifiers: chr4:g.84200178A>C (hg19) ; chr4:g.83279025A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.83279025A>C , CM000666.2:g.83279025A>C	GRCh38
NC_000004.11:g.84200178A>C , CM000666.1:g.84200178A>C	GRCh37
NC_000004.10:g.84419202A>C	NCBI36
NG_015825.1:g.10890T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311469.9:c.493T>G	ENSP00000310873.4:p.Phe165Val
ENST00000647002.2:c.343T>G MANE Select	ENSP00000495761.2:p.Phe115Val
ENST00000311461.7:c.343T>G	ENSP00000311835.7:p.Phe115Val
ENST00000311469.8:c.493T>G	ENSP00000310873.4:p.Phe165Val
ENST00000503391.5:c.343T>G	ENSP00000426242.1:p.Phe115Val
ENST00000503915.5:c.34T>G	ENSP00000427146.1:p.Phe12Val
ENST00000514935.1:n.255T>G
NM_015697.7:c.493T>G	NP_056512.5:p.Phe165Val
XM_011531855.1:c.493T>G	XP_011530157.1:p.Phe165Val
XM_011531856.1:c.493T>G	XP_011530158.1:p.Phe165Val
XM_011531857.1:c.493T>G	XP_011530159.1:p.Phe165Val
XM_011531858.1:c.493T>G	XP_011530160.1:p.Phe165Val
XM_011531859.1:c.493T>G	XP_011530161.1:p.Phe165Val
XM_011531860.1:c.493T>G	XP_011530162.1:p.Phe165Val
XM_011531861.1:c.493T>G	XP_011530163.1:p.Phe165Val
XM_011531862.1:c.493T>G	XP_011530164.1:p.Phe165Val
XM_011531863.1:c.493T>G	XP_011530165.1:p.Phe165Val
XM_011531864.1:c.493T>G	XP_011530166.1:p.Phe165Val
XM_011531865.1:c.493T>G	XP_011530167.1:p.Phe165Val
XM_011531866.1:c.493T>G	XP_011530168.1:p.Phe165Val
XM_011531867.1:c.139T>G	XP_011530169.1:p.Phe47Val
XR_427543.2:n.652T>G
XR_938721.1:n.668T>G
NM_001358921.1:c.343T>G	NP_001345850.1:p.Phe115Val
NM_015697.8:c.493T>G	NP_056512.5:p.Phe165Val
XM_011531855.3:c.343T>G	XP_011530157.2:p.Phe115Val
XM_011531857.3:c.343T>G	XP_011530159.2:p.Phe115Val
XM_011531859.3:c.343T>G	XP_011530161.2:p.Phe115Val
XM_011531860.3:c.343T>G	XP_011530162.2:p.Phe115Val
XM_011531862.3:c.343T>G	XP_011530164.2:p.Phe115Val
XM_011531863.3:c.343T>G	XP_011530165.2:p.Phe115Val
XM_011531866.3:c.343T>G	XP_011530168.2:p.Phe115Val
XM_011531867.3:c.139T>G	XP_011530169.1:p.Phe47Val
XM_017008031.2:c.139T>G	XP_016863520.1:p.Phe47Val
XR_001741203.2:n.374T>G
XR_001741204.2:n.374T>G
XR_427543.4:n.374T>G
XR_938721.3:n.374T>G
NM_001358921.2:c.343T>G MANE Select	NP_001345850.1:p.Phe115Val
NM_015697.9:c.493T>G	NP_056512.5:p.Phe165Val