Canonical Allele Identifier: CA1425385

Gene: COQ8A

Linked Data

• ClinVar Variation Id: 296019
• ClinVar RCV Id: RCV000271765 ; RCV000359320
• dbSNP Id: rs564593360
• ExAC: 1:227171566 C / G
• gnomAD v2: 1-227171566-C-G
• gnomAD v3: 1-226983865-C-G
• gnomAD v4: 1-226983865-C-G
• MyVariant Identifiers: chr1:g.227171566C>G (hg19) ; chr1:g.226983865C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226983865C>G , CM000663.2:g.226983865C>G	GRCh38
NC_000001.10:g.227171566C>G , CM000663.1:g.227171566C>G	GRCh37
NC_000001.9:g.225238189C>G	NCBI36
NG_012825.1:g.48629C>G
NG_012825.2:g.91330C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366777.4:c.1256+11C>G MANE Select	ENSP00000355739.3:n.1256+11C>G
ENST00000366779.6:c.*5983+11C>G	ENSP00000355741.2:n.*5983+11C>G
ENST00000366777.3:c.1256+11C>G	ENSP00000355739.3:n.1256+11C>G
ENST00000366778.5:c.1100+11C>G	ENSP00000355740.1:n.1100+11C>G
ENST00000366779.5:c.1256+11C>G	ENSP00000355741.1:n.1256+11C>G
ENST00000478406.5:n.1890C>G
ENST00000479852.1:n.215C>G
ENST00000485462.5:n.646+11C>G
NM_020247.4:c.1256+11C>G	NP_064632.2:n.1256+11C>G
XM_005273201.1:c.1256+11C>G	XP_005273258.1:n.1256+11C>G
XM_011544238.1:c.1256+11C>G	XP_011542540.1:n.1256+11C>G
XM_011544239.1:c.1256+11C>G	XP_011542541.1:n.1256+11C>G
XM_011544240.1:c.1256+11C>G	XP_011542542.1:n.1256+11C>G
XM_011544241.1:c.1256+11C>G	XP_011542543.1:n.1256+11C>G
XM_011544239.2:c.1256+11C>G	XP_011542541.1:n.1256+11C>G
XM_011544241.2:c.1256+11C>G	XP_011542543.1:n.1256+11C>G
XM_017001852.1:c.1256+11C>G	XP_016857341.1:n.1256+11C>G
XM_024448517.1:c.1256+11C>G	XP_024304285.1:n.1256+11C>G
XM_024448518.1:c.1256+11C>G	XP_024304286.1:n.1256+11C>G
NM_020247.5:c.1256+11C>G MANE Select	NP_064632.2:n.1256+11C>G