Canonical Allele Identifier: CA1225123918

Gene: COQ8A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226983767_226983768delinsTC , CM000663.2:g.226983767_226983768delinsTC	GRCh38
NC_000001.10:g.227171468_227171469delinsTC , CM000663.1:g.227171468_227171469delinsTC	GRCh37
NC_000001.9:g.225238091_225238092delinsTC	NCBI36
NG_012825.1:g.48531_48532delinsTC
NG_012825.2:g.91232_91233delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.1169_1170delinsTC MANE Select	ENSP00000355739.3:p.Phe390=
ENST00000366779.6:c.*5896_*5897delinsTC	ENSP00000355741.2:n.*5896_*5897delinsTC
ENST00000676884.1:c.*6018_*6019delinsTC	ENSP00000503200.1:n.*6018_*6019delinsTC
ENST00000366777.3:c.1169_1170delinsTC	ENSP00000355739.3:p.Phe390=
ENST00000366778.5:c.1013_1014delinsTC	ENSP00000355740.1:p.Phe338=
ENST00000366779.5:c.1169_1170delinsTC	ENSP00000355741.1:p.Phe390=
ENST00000478406.5:n.1792_1793delinsTC
ENST00000479852.1:n.117_118delinsTC
ENST00000485462.5:n.559_560delinsTC
NM_020247.4:c.1169_1170delinsTC	NP_064632.2:p.Phe390=
XM_005273201.1:c.1169_1170delinsTC	XP_005273258.1:p.Phe390=
XM_011544238.1:c.1169_1170delinsTC	XP_011542540.1:p.Phe390=
XM_011544239.1:c.1169_1170delinsTC	XP_011542541.1:p.Phe390=
XM_011544240.1:c.1169_1170delinsTC	XP_011542542.1:p.Phe390=
XM_011544241.1:c.1169_1170delinsTC	XP_011542543.1:p.Phe390=
XM_011544239.2:c.1169_1170delinsTC	XP_011542541.1:p.Phe390=
XM_011544241.2:c.1169_1170delinsTC	XP_011542543.1:p.Phe390=
XM_017001852.1:c.1169_1170delinsTC	XP_016857341.1:p.Phe390=
XM_024448517.1:c.1169_1170delinsTC	XP_024304285.1:p.Phe390=
XM_024448518.1:c.1169_1170delinsTC	XP_024304286.1:p.Phe390=
NM_020247.5:c.1169_1170delinsTC MANE Select	NP_064632.2:p.Phe390=