Canonical Allele Identifier: CA1148418622
Gene: COQ8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226982754G= , CM000663.2:g.226982754G= GRCh38
NC_000001.10:g.227170455G= , CM000663.1:g.227170455G= GRCh37
NC_000001.9:g.225237078G= NCBI36
NG_012825.1:g.47518G=
NG_012825.2:g.90219G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366777.4:c.930G= MANE Select ENSP00000355739.3:p.Lys310=
ENST00000366779.6:c.*5657G= ENSP00000355741.2:n.*5657G=
ENST00000676884.1:c.*5779G= ENSP00000503200.1:n.*5779G=
ENST00000366777.3:c.930G= ENSP00000355739.3:p.Lys310=
ENST00000366778.5:c.774G= ENSP00000355740.1:p.Lys258=
ENST00000366779.5:c.930G= ENSP00000355741.1:p.Lys310=
ENST00000478406.5:n.909G=
ENST00000485462.5:n.320G=
NM_020247.4:c.930G= NP_064632.2:p.Lys310=
XM_005273201.1:c.930G= XP_005273258.1:p.Lys310=
XM_011544238.1:c.930G= XP_011542540.1:p.Lys310=
XM_011544239.1:c.930G= XP_011542541.1:p.Lys310=
XM_011544240.1:c.930G= XP_011542542.1:p.Lys310=
XM_011544241.1:c.930G= XP_011542543.1:p.Lys310=
XM_011544239.2:c.930G= XP_011542541.1:p.Lys310=
XM_011544241.2:c.930G= XP_011542543.1:p.Lys310=
XM_017001852.1:c.930G= XP_016857341.1:p.Lys310=
XM_024448517.1:c.930G= XP_024304285.1:p.Lys310=
XM_024448518.1:c.930G= XP_024304286.1:p.Lys310=
NM_020247.5:c.930G= MANE Select NP_064632.2:p.Lys310=