Canonical Allele Identifier: CA423528355

Gene: COQ8A

Linked Data

• dbSNP Id: rs1190712859
• gnomAD v2: 1-227172279-A-C
• gnomAD v4: 1-226984578-A-C
• MyVariant Identifiers: chr1:g.227172279A>C (hg19) ; chr1:g.226984578A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226984578A>C , CM000663.2:g.226984578A>C	GRCh38
NC_000001.10:g.227172279A>C , CM000663.1:g.227172279A>C	GRCh37
NC_000001.9:g.225238902A>C	NCBI36
NG_012825.1:g.49342A>C
NG_012825.2:g.92043A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.1429A>C MANE Select	ENSP00000355739.3:p.Arg477=
ENST00000366779.6:c.*6156A>C	ENSP00000355741.2:n.*6156A>C
ENST00000366777.3:c.1429A>C	ENSP00000355739.3:p.Arg477=
ENST00000366778.5:c.1273A>C	ENSP00000355740.1:p.Arg425=
ENST00000366779.5:c.1429A>C	ENSP00000355741.1:p.Arg477=
ENST00000478406.5:n.2291A>C
ENST00000479852.1:n.616A>C
ENST00000485462.5:n.819A>C
NM_020247.4:c.1429A>C	NP_064632.2:p.Arg477=
XM_005273201.1:c.1429A>C	XP_005273258.1:p.Arg477=
XM_011544238.1:c.1429A>C	XP_011542540.1:p.Arg477=
XM_011544239.1:c.1429A>C	XP_011542541.1:p.Arg477=
XM_011544240.1:c.1429A>C	XP_011542542.1:p.Arg477=
XM_011544241.1:c.1429A>C	XP_011542543.1:p.Arg477=
XM_011544239.2:c.1429A>C	XP_011542541.1:p.Arg477=
XM_011544241.2:c.1429A>C	XP_011542543.1:p.Arg477=
XM_017001852.1:c.1429A>C	XP_016857341.1:p.Arg477=
XM_024448517.1:c.1429A>C	XP_024304285.1:p.Arg477=
XM_024448518.1:c.1429A>C	XP_024304286.1:p.Arg477=
NM_020247.5:c.1429A>C MANE Select	NP_064632.2:p.Arg477=