Canonical Allele Identifier: CA290432

Gene: COQ2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.83284842A>C , CM000666.2:g.83284842A>C	GRCh38
NC_000004.11:g.84205995A>C , CM000666.1:g.84205995A>C	GRCh37
NC_000004.10:g.84425019A>C	NCBI36
NG_015825.1:g.5073T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311469.9:c.73T>G	ENSP00000310873.4:p.Leu25Val
ENST00000311469.8:c.73T>G	ENSP00000310873.4:p.Leu25Val
NM_015697.7:c.73T>G	NP_056512.5:p.Leu25Val
XM_011531855.1:c.73T>G	XP_011530157.1:p.Leu25Val
XM_011531856.1:c.73T>G	XP_011530158.1:p.Leu25Val
XM_011531857.1:c.73T>G	XP_011530159.1:p.Leu25Val
XM_011531858.1:c.73T>G	XP_011530160.1:p.Leu25Val
XM_011531859.1:c.73T>G	XP_011530161.1:p.Leu25Val
XM_011531860.1:c.73T>G	XP_011530162.1:p.Leu25Val
XM_011531861.1:c.73T>G	XP_011530163.1:p.Leu25Val
XM_011531862.1:c.73T>G	XP_011530164.1:p.Leu25Val
XM_011531863.1:c.73T>G	XP_011530165.1:p.Leu25Val
XM_011531864.1:c.73T>G	XP_011530166.1:p.Leu25Val
XM_011531865.1:c.73T>G	XP_011530167.1:p.Leu25Val
XM_011531866.1:c.73T>G	XP_011530168.1:p.Leu25Val
XR_427543.2:n.232T>G
XR_938721.1:n.248T>G
NM_015697.8:c.73T>G	NP_056512.5:p.Leu25Val
NM_015697.9:c.73T>G	NP_056512.5:p.Leu25Val