Canonical Allele Identifier: CA38644342

Gene: COQ8A

Linked Data

• ClinVar Variation Id: 1984006
• ClinVar RCV Id: RCV002756711
• dbSNP Id: rs1042812307
• gnomAD v4: 1-226982022-C-T
• MyVariant Identifiers: chr1:g.227169723C>T (hg19) ; chr1:g.226982022C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226982022C>T , CM000663.2:g.226982022C>T	GRCh38
NC_000001.10:g.227169723C>T , CM000663.1:g.227169723C>T	GRCh37
NC_000001.9:g.225236346C>T	NCBI36
NG_012825.1:g.46786C>T
NG_012825.2:g.89487C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.731-5C>T MANE Select	ENSP00000355739.3:n.731-5C>T
ENST00000366779.6:c.*5458-5C>T	ENSP00000355741.2:n.*5458-5C>T
ENST00000676884.1:c.*5580-5C>T	ENSP00000503200.1:n.*5580-5C>T
ENST00000366777.3:c.731-5C>T	ENSP00000355739.3:n.731-5C>T
ENST00000366778.5:c.575-5C>T	ENSP00000355740.1:n.575-5C>T
ENST00000366779.5:c.731-5C>T	ENSP00000355741.1:n.731-5C>T
ENST00000478406.5:n.182-5C>T
ENST00000485462.5:n.121-5C>T
NM_020247.4:c.731-5C>T	NP_064632.2:n.731-5C>T
XM_005273201.1:c.731-5C>T	XP_005273258.1:n.731-5C>T
XM_011544238.1:c.731-5C>T	XP_011542540.1:n.731-5C>T
XM_011544239.1:c.731-5C>T	XP_011542541.1:n.731-5C>T
XM_011544240.1:c.731-5C>T	XP_011542542.1:n.731-5C>T
XM_011544241.1:c.731-5C>T	XP_011542543.1:n.731-5C>T
XM_011544239.2:c.731-5C>T	XP_011542541.1:n.731-5C>T
XM_011544241.2:c.731-5C>T	XP_011542543.1:n.731-5C>T
XM_017001852.1:c.731-5C>T	XP_016857341.1:n.731-5C>T
XM_024448517.1:c.731-5C>T	XP_024304285.1:n.731-5C>T
XM_024448518.1:c.731-5C>T	XP_024304286.1:n.731-5C>T
NM_020247.5:c.731-5C>T MANE Select	NP_064632.2:n.731-5C>T