Canonical Allele Identifier: CA1142487100
Gene: COQ8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226982974C= , CM000663.2:g.226982974C= GRCh38
NC_000001.10:g.227170675C= , CM000663.1:g.227170675C= GRCh37
NC_000001.9:g.225237298C= NCBI36
NG_012825.1:g.47738C=
NG_012825.2:g.90439C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366777.4:c.1020C= MANE Select ENSP00000355739.3:p.Ser340=
ENST00000366779.6:c.*5747C= ENSP00000355741.2:n.*5747C=
ENST00000676884.1:c.*5869C= ENSP00000503200.1:n.*5869C=
ENST00000366777.3:c.1020C= ENSP00000355739.3:p.Ser340=
ENST00000366778.5:c.864C= ENSP00000355740.1:p.Ser288=
ENST00000366779.5:c.1020C= ENSP00000355741.1:p.Ser340=
ENST00000478406.5:n.999C=
ENST00000485462.5:n.410C=
NM_020247.4:c.1020C= NP_064632.2:p.Ser340=
XM_005273201.1:c.1020C= XP_005273258.1:p.Ser340=
XM_011544238.1:c.1020C= XP_011542540.1:p.Ser340=
XM_011544239.1:c.1020C= XP_011542541.1:p.Ser340=
XM_011544240.1:c.1020C= XP_011542542.1:p.Ser340=
XM_011544241.1:c.1020C= XP_011542543.1:p.Ser340=
XM_011544239.2:c.1020C= XP_011542541.1:p.Ser340=
XM_011544241.2:c.1020C= XP_011542543.1:p.Ser340=
XM_017001852.1:c.1020C= XP_016857341.1:p.Ser340=
XM_024448517.1:c.1020C= XP_024304285.1:p.Ser340=
XM_024448518.1:c.1020C= XP_024304286.1:p.Ser340=
NM_020247.5:c.1020C= MANE Select NP_064632.2:p.Ser340=