Canonical Allele Identifier: CA1225124504

Gene: COQ8A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226984853_226984856delinsTCTC , CM000663.2:g.226984853_226984856delinsTCTC	GRCh38
NC_000001.10:g.227172554_227172557delinsTCTC , CM000663.1:g.227172554_227172557delinsTCTC	GRCh37
NC_000001.9:g.225239177_225239180delinsTCTC	NCBI36
NG_012825.1:g.49617_49620delinsTCTC
NG_012825.2:g.92318_92321delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.1507-23_1507-20delinsTCTC MANE Select	ENSP00000355739.3:n.1507-23_1507-20delinsTCTC
ENST00000366779.6:c.*6234-23_*6234-20delinsTCTC	ENSP00000355741.2:n.*6234-23_*6234-20delinsTCTC
ENST00000366777.3:c.1507-23_1507-20delinsTCTC	ENSP00000355739.3:n.1507-23_1507-20delinsTCTC
ENST00000366778.5:c.1351-23_1351-20delinsTCTC	ENSP00000355740.1:n.1351-23_1351-20delinsTCTC
ENST00000366779.5:c.1507-23_1507-20delinsTCTC	ENSP00000355741.1:n.1507-23_1507-20delinsTCTC
ENST00000478406.5:n.2369-23_2369-20delinsTCTC
ENST00000479852.1:n.694-23_694-20delinsTCTC
ENST00000485462.5:n.897-23_897-20delinsTCTC
NM_020247.4:c.1507-23_1507-20delinsTCTC	NP_064632.2:n.1507-23_1507-20delinsTCTC
XM_005273201.1:c.1507-23_1507-20delinsTCTC	XP_005273258.1:n.1507-23_1507-20delinsTCTC
XM_011544238.1:c.1507-23_1507-20delinsTCTC	XP_011542540.1:n.1507-23_1507-20delinsTCTC
XM_011544239.1:c.1507-23_1507-20delinsTCTC	XP_011542541.1:n.1507-23_1507-20delinsTCTC
XM_011544240.1:c.1507-23_1507-20delinsTCTC	XP_011542542.1:n.1507-23_1507-20delinsTCTC
XM_011544241.1:c.1507-23_1507-20delinsTCTC	XP_011542543.1:n.1507-23_1507-20delinsTCTC
XM_011544239.2:c.1507-23_1507-20delinsTCTC	XP_011542541.1:n.1507-23_1507-20delinsTCTC
XM_011544241.2:c.1507-23_1507-20delinsTCTC	XP_011542543.1:n.1507-23_1507-20delinsTCTC
XM_017001852.1:c.1507-23_1507-20delinsTCTC	XP_016857341.1:n.1507-23_1507-20delinsTCTC
XM_024448517.1:c.1507-23_1507-20delinsTCTC	XP_024304285.1:n.1507-23_1507-20delinsTCTC
XM_024448518.1:c.1507-23_1507-20delinsTCTC	XP_024304286.1:n.1507-23_1507-20delinsTCTC
NM_020247.5:c.1507-23_1507-20delinsTCTC MANE Select	NP_064632.2:n.1507-23_1507-20delinsTCTC