Canonical Allele Identifier: CA38644665

Gene: COQ8A

Linked Data

• ClinVar Variation Id: 679657
• ClinVar RCV Id: RCV000839352
• dbSNP Id: rs76213739
• gnomAD v2: 1-227170006-G-A
• gnomAD v3: 1-226982305-G-A
• gnomAD v4: 1-226982305-G-A
• MyVariant Identifiers: chr1:g.227170006G>A (hg19) ; chr1:g.226982305G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226982305G>A , CM000663.2:g.226982305G>A	GRCh38
NC_000001.10:g.227170006G>A , CM000663.1:g.227170006G>A	GRCh37
NC_000001.9:g.225236629G>A	NCBI36
NG_012825.1:g.47069G>A
NG_012825.2:g.89770G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.853+156G>A MANE Select	ENSP00000355739.3:n.853+156G>A
ENST00000366779.6:c.*5580+156G>A	ENSP00000355741.2:n.*5580+156G>A
ENST00000676884.1:c.*5702+156G>A	ENSP00000503200.1:n.*5702+156G>A
ENST00000366777.3:c.853+156G>A	ENSP00000355739.3:n.853+156G>A
ENST00000366778.5:c.697+156G>A	ENSP00000355740.1:n.697+156G>A
ENST00000366779.5:c.853+156G>A	ENSP00000355741.1:n.853+156G>A
ENST00000478406.5:n.460G>A
ENST00000485462.5:n.243+156G>A
NM_020247.4:c.853+156G>A	NP_064632.2:n.853+156G>A
XM_005273201.1:c.853+156G>A	XP_005273258.1:n.853+156G>A
XM_011544238.1:c.853+156G>A	XP_011542540.1:n.853+156G>A
XM_011544239.1:c.853+156G>A	XP_011542541.1:n.853+156G>A
XM_011544240.1:c.853+156G>A	XP_011542542.1:n.853+156G>A
XM_011544241.1:c.853+156G>A	XP_011542543.1:n.853+156G>A
XM_011544239.2:c.853+156G>A	XP_011542541.1:n.853+156G>A
XM_011544241.2:c.853+156G>A	XP_011542543.1:n.853+156G>A
XM_017001852.1:c.853+156G>A	XP_016857341.1:n.853+156G>A
XM_024448517.1:c.853+156G>A	XP_024304285.1:n.853+156G>A
XM_024448518.1:c.853+156G>A	XP_024304286.1:n.853+156G>A
NM_020247.5:c.853+156G>A MANE Select	NP_064632.2:n.853+156G>A