Canonical Allele Identifier: CA1143784610

Gene: COQ8A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226984405_226984407delinsCCC , CM000663.2:g.226984405_226984407delinsCCC	GRCh38
NC_000001.10:g.227172106_227172108delinsCCC , CM000663.1:g.227172106_227172108delinsCCC	GRCh37
NC_000001.9:g.225238729_225238731delinsCCC	NCBI36
NG_012825.1:g.49169_49171delinsCCC
NG_012825.2:g.91870_91872delinsCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.1399-143_1399-141delinsCCC MANE Select	ENSP00000355739.3:n.1399-143_1399-141delinsCCC
ENST00000366779.6:c.*6126-143_*6126-141delinsCCC	ENSP00000355741.2:n.*6126-143_*6126-141delinsCCC
ENST00000366777.3:c.1399-143_1399-141delinsCCC	ENSP00000355739.3:n.1399-143_1399-141delinsCCC
ENST00000366778.5:c.1243-143_1243-141delinsCCC	ENSP00000355740.1:n.1243-143_1243-141delinsCCC
ENST00000366779.5:c.1399-143_1399-141delinsCCC	ENSP00000355741.1:n.1399-143_1399-141delinsCCC
ENST00000478406.5:n.2261-143_2261-141delinsCCC
ENST00000479852.1:n.586-143_586-141delinsCCC
ENST00000485462.5:n.789-143_789-141delinsCCC
NM_020247.4:c.1399-143_1399-141delinsCCC	NP_064632.2:n.1399-143_1399-141delinsCCC
XM_005273201.1:c.1399-143_1399-141delinsCCC	XP_005273258.1:n.1399-143_1399-141delinsCCC
XM_011544238.1:c.1399-143_1399-141delinsCCC	XP_011542540.1:n.1399-143_1399-141delinsCCC
XM_011544239.1:c.1399-143_1399-141delinsCCC	XP_011542541.1:n.1399-143_1399-141delinsCCC
XM_011544240.1:c.1399-143_1399-141delinsCCC	XP_011542542.1:n.1399-143_1399-141delinsCCC
XM_011544241.1:c.1399-143_1399-141delinsCCC	XP_011542543.1:n.1399-143_1399-141delinsCCC
XM_011544239.2:c.1399-143_1399-141delinsCCC	XP_011542541.1:n.1399-143_1399-141delinsCCC
XM_011544241.2:c.1399-143_1399-141delinsCCC	XP_011542543.1:n.1399-143_1399-141delinsCCC
XM_017001852.1:c.1399-143_1399-141delinsCCC	XP_016857341.1:n.1399-143_1399-141delinsCCC
XM_024448517.1:c.1399-143_1399-141delinsCCC	XP_024304285.1:n.1399-143_1399-141delinsCCC
XM_024448518.1:c.1399-143_1399-141delinsCCC	XP_024304286.1:n.1399-143_1399-141delinsCCC
NM_020247.5:c.1399-143_1399-141delinsCCC MANE Select	NP_064632.2:n.1399-143_1399-141delinsCCC