Canonical Allele Identifier: CA1225123476
Gene: COQ8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226982889T= , CM000663.2:g.226982889T= GRCh38
NC_000001.10:g.227170590T= , CM000663.1:g.227170590T= GRCh37
NC_000001.9:g.225237213T= NCBI36
NG_012825.1:g.47653T=
NG_012825.2:g.90354T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366777.4:c.940-5T= MANE Select ENSP00000355739.3:n.940-5T=
ENST00000366779.6:c.*5667-5T= ENSP00000355741.2:n.*5667-5T=
ENST00000676884.1:c.*5789-5T= ENSP00000503200.1:n.*5789-5T=
ENST00000366777.3:c.940-5T= ENSP00000355739.3:n.940-5T=
ENST00000366778.5:c.784-5T= ENSP00000355740.1:n.784-5T=
ENST00000366779.5:c.940-5T= ENSP00000355741.1:n.940-5T=
ENST00000478406.5:n.919-5T=
ENST00000485462.5:n.330-5T=
NM_020247.4:c.940-5T= NP_064632.2:n.940-5T=
XM_005273201.1:c.940-5T= XP_005273258.1:n.940-5T=
XM_011544238.1:c.940-5T= XP_011542540.1:n.940-5T=
XM_011544239.1:c.940-5T= XP_011542541.1:n.940-5T=
XM_011544240.1:c.940-5T= XP_011542542.1:n.940-5T=
XM_011544241.1:c.940-5T= XP_011542543.1:n.940-5T=
XM_011544239.2:c.940-5T= XP_011542541.1:n.940-5T=
XM_011544241.2:c.940-5T= XP_011542543.1:n.940-5T=
XM_017001852.1:c.940-5T= XP_016857341.1:n.940-5T=
XM_024448517.1:c.940-5T= XP_024304285.1:n.940-5T=
XM_024448518.1:c.940-5T= XP_024304286.1:n.940-5T=
NM_020247.5:c.940-5T= MANE Select NP_064632.2:n.940-5T=