Canonical Allele Identifier: CA1225124436
Gene: COQ8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226984713A= , CM000663.2:g.226984713A= GRCh38
NC_000001.10:g.227172414A= , CM000663.1:g.227172414A= GRCh37
NC_000001.9:g.225239037A= NCBI36
NG_012825.1:g.49477A=
NG_012825.2:g.92178A=

Transcript Alleles

HGVS Amino-acid change
ENST00000366777.4:c.1506+58A= MANE Select ENSP00000355739.3:n.1506+58A=
ENST00000366779.6:c.*6233+58A= ENSP00000355741.2:n.*6233+58A=
ENST00000366777.3:c.1506+58A= ENSP00000355739.3:n.1506+58A=
ENST00000366778.5:c.1350+58A= ENSP00000355740.1:n.1350+58A=
ENST00000366779.5:c.1506+58A= ENSP00000355741.1:n.1506+58A=
ENST00000478406.5:n.2368+58A=
ENST00000479852.1:n.693+58A=
ENST00000485462.5:n.896+58A=
NM_020247.4:c.1506+58A= NP_064632.2:n.1506+58A=
XM_005273201.1:c.1506+58A= XP_005273258.1:n.1506+58A=
XM_011544238.1:c.1506+58A= XP_011542540.1:n.1506+58A=
XM_011544239.1:c.1506+58A= XP_011542541.1:n.1506+58A=
XM_011544240.1:c.1506+58A= XP_011542542.1:n.1506+58A=
XM_011544241.1:c.1506+58A= XP_011542543.1:n.1506+58A=
XM_011544239.2:c.1506+58A= XP_011542541.1:n.1506+58A=
XM_011544241.2:c.1506+58A= XP_011542543.1:n.1506+58A=
XM_017001852.1:c.1506+58A= XP_016857341.1:n.1506+58A=
XM_024448517.1:c.1506+58A= XP_024304285.1:n.1506+58A=
XM_024448518.1:c.1506+58A= XP_024304286.1:n.1506+58A=
NM_020247.5:c.1506+58A= MANE Select NP_064632.2:n.1506+58A=