Canonical Allele Identifier: CA2840774882

Gene: COQ8A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226984750C>T , CM000663.2:g.226984750C>T	GRCh38
NC_000001.10:g.227172451C>T , CM000663.1:g.227172451C>T	GRCh37
NC_000001.9:g.225239074C>T	NCBI36
NG_012825.1:g.49514C>T
NG_012825.2:g.92215C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.1506+95C>T MANE Select	ENSP00000355739.3:n.1506+95C>T
ENST00000366779.6:c.*6233+95C>T	ENSP00000355741.2:n.*6233+95C>T
ENST00000366777.3:c.1506+95C>T	ENSP00000355739.3:n.1506+95C>T
ENST00000366778.5:c.1350+95C>T	ENSP00000355740.1:n.1350+95C>T
ENST00000366779.5:c.1506+95C>T	ENSP00000355741.1:n.1506+95C>T
ENST00000478406.5:n.2368+95C>T
ENST00000479852.1:n.693+95C>T
ENST00000485462.5:n.896+95C>T
NM_020247.4:c.1506+95C>T	NP_064632.2:n.1506+95C>T
XM_005273201.1:c.1506+95C>T	XP_005273258.1:n.1506+95C>T
XM_011544238.1:c.1506+95C>T	XP_011542540.1:n.1506+95C>T
XM_011544239.1:c.1506+95C>T	XP_011542541.1:n.1506+95C>T
XM_011544240.1:c.1506+95C>T	XP_011542542.1:n.1506+95C>T
XM_011544241.1:c.1506+95C>T	XP_011542543.1:n.1506+95C>T
XM_011544239.2:c.1506+95C>T	XP_011542541.1:n.1506+95C>T
XM_011544241.2:c.1506+95C>T	XP_011542543.1:n.1506+95C>T
XM_017001852.1:c.1506+95C>T	XP_016857341.1:n.1506+95C>T
XM_024448517.1:c.1506+95C>T	XP_024304285.1:n.1506+95C>T
XM_024448518.1:c.1506+95C>T	XP_024304286.1:n.1506+95C>T
NM_020247.5:c.1506+95C>T MANE Select	NP_064632.2:n.1506+95C>T