Canonical Allele Identifier: CA2671245738

Gene: COQ2

Linked Data

• gnomAD v4: 4-83278909-TGAGAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.83278913_83278917del , CM000666.2:g.83278913_83278917del	GRCh38
NC_000004.11:g.84200066_84200070del , CM000666.1:g.84200066_84200070del	GRCh37
NC_000004.10:g.84419090_84419094del	NCBI36
NG_015825.1:g.11001_11005del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311469.9:c.570+34_570+38del	ENSP00000310873.4:n.570+34_570+38del
ENST00000647002.2:c.420+34_420+38del MANE Select	ENSP00000495761.2:n.420+34_420+38del
ENST00000311461.7:c.420+34_420+38del	ENSP00000311835.7:n.420+34_420+38del
ENST00000311469.8:c.570+34_570+38del	ENSP00000310873.4:n.570+34_570+38del
ENST00000503391.5:c.420+34_420+38del	ENSP00000426242.1:n.420+34_420+38del
ENST00000503915.5:c.111+34_111+38del	ENSP00000427146.1:n.111+34_111+38del
ENST00000514935.1:n.332+34_332+38del
NM_015697.7:c.570+34_570+38del	NP_056512.5:n.570+34_570+38del
XM_011531855.1:c.570+34_570+38del	XP_011530157.1:n.570+34_570+38del
XM_011531856.1:c.570+34_570+38del	XP_011530158.1:n.570+34_570+38del
XM_011531857.1:c.570+34_570+38del	XP_011530159.1:n.570+34_570+38del
XM_011531858.1:c.570+34_570+38del	XP_011530160.1:n.570+34_570+38del
XM_011531859.1:c.570+34_570+38del	XP_011530161.1:n.570+34_570+38del
XM_011531860.1:c.570+34_570+38del	XP_011530162.1:n.570+34_570+38del
XM_011531861.1:c.570+34_570+38del	XP_011530163.1:n.570+34_570+38del
XM_011531862.1:c.570+34_570+38del	XP_011530164.1:n.570+34_570+38del
XM_011531863.1:c.570+34_570+38del	XP_011530165.1:n.570+34_570+38del
XM_011531864.1:c.570+34_570+38del	XP_011530166.1:n.570+34_570+38del
XM_011531865.1:c.570+34_570+38del	XP_011530167.1:n.570+34_570+38del
XM_011531866.1:c.570+34_570+38del	XP_011530168.1:n.570+34_570+38del
XM_011531867.1:c.216+34_216+38del	XP_011530169.1:n.216+34_216+38del
XR_427543.2:n.729+34_729+38del
XR_938721.1:n.745+34_745+38del
NM_001358921.1:c.420+34_420+38del	NP_001345850.1:n.420+34_420+38del
NM_015697.8:c.570+34_570+38del	NP_056512.5:n.570+34_570+38del
XM_011531855.3:c.420+34_420+38del	XP_011530157.2:n.420+34_420+38del
XM_011531857.3:c.420+34_420+38del	XP_011530159.2:n.420+34_420+38del
XM_011531859.3:c.420+34_420+38del	XP_011530161.2:n.420+34_420+38del
XM_011531860.3:c.420+34_420+38del	XP_011530162.2:n.420+34_420+38del
XM_011531862.3:c.420+34_420+38del	XP_011530164.2:n.420+34_420+38del
XM_011531863.3:c.420+34_420+38del	XP_011530165.2:n.420+34_420+38del
XM_011531866.3:c.420+34_420+38del	XP_011530168.2:n.420+34_420+38del
XM_011531867.3:c.216+34_216+38del	XP_011530169.1:n.216+34_216+38del
XM_017008031.2:c.216+34_216+38del	XP_016863520.1:n.216+34_216+38del
XR_001741203.2:n.451+34_451+38del
XR_001741204.2:n.451+34_451+38del
XR_427543.4:n.451+34_451+38del
XR_938721.3:n.451+34_451+38del
NM_001358921.2:c.420+34_420+38del MANE Select	NP_001345850.1:n.420+34_420+38del
NM_015697.9:c.570+34_570+38del	NP_056512.5:n.570+34_570+38del