Canonical Allele Identifier: CA357230628

Gene: COQ2

Linked Data

• gnomAD v4: 4-83279050-A-T
• MyVariant Identifiers: chr4:g.84200203A>T (hg19) ; chr4:g.83279050A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.83279050A>T , CM000666.2:g.83279050A>T	GRCh38
NC_000004.11:g.84200203A>T , CM000666.1:g.84200203A>T	GRCh37
NC_000004.10:g.84419227A>T	NCBI36
NG_015825.1:g.10865T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311469.9:c.468T>A	ENSP00000310873.4:p.Phe156Leu
ENST00000647002.2:c.318T>A MANE Select	ENSP00000495761.2:p.Phe106Leu
ENST00000311461.7:c.318T>A	ENSP00000311835.7:p.Phe106Leu
ENST00000311469.8:c.468T>A	ENSP00000310873.4:p.Phe156Leu
ENST00000503391.5:c.318T>A	ENSP00000426242.1:p.Phe106Leu
ENST00000503915.5:c.9T>A	ENSP00000427146.1:p.Phe3Leu
ENST00000514935.1:n.230T>A
NM_015697.7:c.468T>A	NP_056512.5:p.Phe156Leu
XM_011531855.1:c.468T>A	XP_011530157.1:p.Phe156Leu
XM_011531856.1:c.468T>A	XP_011530158.1:p.Phe156Leu
XM_011531857.1:c.468T>A	XP_011530159.1:p.Phe156Leu
XM_011531858.1:c.468T>A	XP_011530160.1:p.Phe156Leu
XM_011531859.1:c.468T>A	XP_011530161.1:p.Phe156Leu
XM_011531860.1:c.468T>A	XP_011530162.1:p.Phe156Leu
XM_011531861.1:c.468T>A	XP_011530163.1:p.Phe156Leu
XM_011531862.1:c.468T>A	XP_011530164.1:p.Phe156Leu
XM_011531863.1:c.468T>A	XP_011530165.1:p.Phe156Leu
XM_011531864.1:c.468T>A	XP_011530166.1:p.Phe156Leu
XM_011531865.1:c.468T>A	XP_011530167.1:p.Phe156Leu
XM_011531866.1:c.468T>A	XP_011530168.1:p.Phe156Leu
XM_011531867.1:c.114T>A	XP_011530169.1:p.Phe38Leu
XR_427543.2:n.627T>A
XR_938721.1:n.643T>A
NM_001358921.1:c.318T>A	NP_001345850.1:p.Phe106Leu
NM_015697.8:c.468T>A	NP_056512.5:p.Phe156Leu
XM_011531855.3:c.318T>A	XP_011530157.2:p.Phe106Leu
XM_011531857.3:c.318T>A	XP_011530159.2:p.Phe106Leu
XM_011531859.3:c.318T>A	XP_011530161.2:p.Phe106Leu
XM_011531860.3:c.318T>A	XP_011530162.2:p.Phe106Leu
XM_011531862.3:c.318T>A	XP_011530164.2:p.Phe106Leu
XM_011531863.3:c.318T>A	XP_011530165.2:p.Phe106Leu
XM_011531866.3:c.318T>A	XP_011530168.2:p.Phe106Leu
XM_011531867.3:c.114T>A	XP_011530169.1:p.Phe38Leu
XM_017008031.2:c.114T>A	XP_016863520.1:p.Phe38Leu
XR_001741203.2:n.349T>A
XR_001741204.2:n.349T>A
XR_427543.4:n.349T>A
XR_938721.3:n.349T>A
NM_001358921.2:c.318T>A MANE Select	NP_001345850.1:p.Phe106Leu
NM_015697.9:c.468T>A	NP_056512.5:p.Phe156Leu