Canonical Allele Identifier: CA1225124264

Gene: COQ8A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226984404_226984406delinsTCC , CM000663.2:g.226984404_226984406delinsTCC	GRCh38
NC_000001.10:g.227172105_227172107delinsTCC , CM000663.1:g.227172105_227172107delinsTCC	GRCh37
NC_000001.9:g.225238728_225238730delinsTCC	NCBI36
NG_012825.1:g.49168_49170delinsTCC
NG_012825.2:g.91869_91871delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.1399-144_1399-142delinsTCC MANE Select	ENSP00000355739.3:n.1399-144_1399-142delinsTCC
ENST00000366779.6:c.*6126-144_*6126-142delinsTCC	ENSP00000355741.2:n.*6126-144_*6126-142delinsTCC
ENST00000366777.3:c.1399-144_1399-142delinsTCC	ENSP00000355739.3:n.1399-144_1399-142delinsTCC
ENST00000366778.5:c.1243-144_1243-142delinsTCC	ENSP00000355740.1:n.1243-144_1243-142delinsTCC
ENST00000366779.5:c.1399-144_1399-142delinsTCC	ENSP00000355741.1:n.1399-144_1399-142delinsTCC
ENST00000478406.5:n.2261-144_2261-142delinsTCC
ENST00000479852.1:n.586-144_586-142delinsTCC
ENST00000485462.5:n.789-144_789-142delinsTCC
NM_020247.4:c.1399-144_1399-142delinsTCC	NP_064632.2:n.1399-144_1399-142delinsTCC
XM_005273201.1:c.1399-144_1399-142delinsTCC	XP_005273258.1:n.1399-144_1399-142delinsTCC
XM_011544238.1:c.1399-144_1399-142delinsTCC	XP_011542540.1:n.1399-144_1399-142delinsTCC
XM_011544239.1:c.1399-144_1399-142delinsTCC	XP_011542541.1:n.1399-144_1399-142delinsTCC
XM_011544240.1:c.1399-144_1399-142delinsTCC	XP_011542542.1:n.1399-144_1399-142delinsTCC
XM_011544241.1:c.1399-144_1399-142delinsTCC	XP_011542543.1:n.1399-144_1399-142delinsTCC
XM_011544239.2:c.1399-144_1399-142delinsTCC	XP_011542541.1:n.1399-144_1399-142delinsTCC
XM_011544241.2:c.1399-144_1399-142delinsTCC	XP_011542543.1:n.1399-144_1399-142delinsTCC
XM_017001852.1:c.1399-144_1399-142delinsTCC	XP_016857341.1:n.1399-144_1399-142delinsTCC
XM_024448517.1:c.1399-144_1399-142delinsTCC	XP_024304285.1:n.1399-144_1399-142delinsTCC
XM_024448518.1:c.1399-144_1399-142delinsTCC	XP_024304286.1:n.1399-144_1399-142delinsTCC
NM_020247.5:c.1399-144_1399-142delinsTCC MANE Select	NP_064632.2:n.1399-144_1399-142delinsTCC