Canonical Allele Identifier: CA1225114669
Gene: COQ8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226965657T= , CM000663.2:g.226965657T= GRCh38
NC_000001.10:g.227153358T= , CM000663.1:g.227153358T= GRCh37
NC_000001.9:g.225219981T= NCBI36
NG_012825.1:g.30421T=
NG_012825.2:g.73122T=

Transcript Alleles

HGVS Amino-acid change
ENST00000366777.4:c.589-14T= MANE Select ENSP00000355739.3:n.589-14T=
ENST00000366779.6:c.*5316-14T= ENSP00000355741.2:n.*5316-14T=
ENST00000676884.1:c.*5438-14T= ENSP00000503200.1:n.*5438-14T=
ENST00000366777.3:c.589-14T= ENSP00000355739.3:n.589-14T=
ENST00000366778.5:c.433-14T= ENSP00000355740.1:n.433-14T=
ENST00000366779.5:c.589-14T= ENSP00000355741.1:n.589-14T=
ENST00000478406.5:n.107-11792T=
ENST00000489044.1:n.800-14T=
NM_020247.4:c.589-14T= NP_064632.2:n.589-14T=
XM_005273201.1:c.589-14T= XP_005273258.1:n.589-14T=
XM_011544238.1:c.589-14T= XP_011542540.1:n.589-14T=
XM_011544239.1:c.589-14T= XP_011542541.1:n.589-14T=
XM_011544240.1:c.589-14T= XP_011542542.1:n.589-14T=
XM_011544241.1:c.589-14T= XP_011542543.1:n.589-14T=
XM_011544239.2:c.589-14T= XP_011542541.1:n.589-14T=
XM_011544241.2:c.589-14T= XP_011542543.1:n.589-14T=
XM_017001852.1:c.589-14T= XP_016857341.1:n.589-14T=
XM_024448517.1:c.589-14T= XP_024304285.1:n.589-14T=
XM_024448518.1:c.589-14T= XP_024304286.1:n.589-14T=
NM_020247.5:c.589-14T= MANE Select NP_064632.2:n.589-14T=