Canonical Allele Identifier: CA1225123483

Gene: COQ8A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226982905C= , CM000663.2:g.226982905C=	GRCh38
NC_000001.10:g.227170606C= , CM000663.1:g.227170606C=	GRCh37
NC_000001.9:g.225237229C=	NCBI36
NG_012825.1:g.47669C=
NG_012825.2:g.90370C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.951C= MANE Select	ENSP00000355739.3:p.Asn317=
ENST00000366779.6:c.*5678C=	ENSP00000355741.2:n.*5678C=
ENST00000676884.1:c.*5800C=	ENSP00000503200.1:n.*5800C=
ENST00000366777.3:c.951C=	ENSP00000355739.3:p.Asn317=
ENST00000366778.5:c.795C=	ENSP00000355740.1:p.Asn265=
ENST00000366779.5:c.951C=	ENSP00000355741.1:p.Asn317=
ENST00000478406.5:n.930C=
ENST00000485462.5:n.341C=
NM_020247.4:c.951C=	NP_064632.2:p.Asn317=
XM_005273201.1:c.951C=	XP_005273258.1:p.Asn317=
XM_011544238.1:c.951C=	XP_011542540.1:p.Asn317=
XM_011544239.1:c.951C=	XP_011542541.1:p.Asn317=
XM_011544240.1:c.951C=	XP_011542542.1:p.Asn317=
XM_011544241.1:c.951C=	XP_011542543.1:p.Asn317=
XM_011544239.2:c.951C=	XP_011542541.1:p.Asn317=
XM_011544241.2:c.951C=	XP_011542543.1:p.Asn317=
XM_017001852.1:c.951C=	XP_016857341.1:p.Asn317=
XM_024448517.1:c.951C=	XP_024304285.1:p.Asn317=
XM_024448518.1:c.951C=	XP_024304286.1:p.Asn317=
NM_020247.5:c.951C= MANE Select	NP_064632.2:p.Asn317=