Canonical Allele Identifier: CA2650793087

Gene: COQ8A

Linked Data

• gnomAD v4: 1-226982396-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226982400del , CM000663.2:g.226982400del	GRCh38
NC_000001.10:g.227170101del , CM000663.1:g.227170101del	GRCh37
NC_000001.9:g.225236724del	NCBI36
NG_012825.1:g.47164del
NG_012825.2:g.89865del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.853+251del MANE Select	ENSP00000355739.3:n.853+251del
ENST00000366779.6:c.*5580+251del	ENSP00000355741.2:n.*5580+251del
ENST00000676884.1:c.*5702+251del	ENSP00000503200.1:n.*5702+251del
ENST00000366777.3:c.853+251del	ENSP00000355739.3:n.853+251del
ENST00000366778.5:c.697+251del	ENSP00000355740.1:n.697+251del
ENST00000366779.5:c.853+251del	ENSP00000355741.1:n.853+251del
ENST00000478406.5:n.555del
ENST00000485462.5:n.243+251del
NM_020247.4:c.853+251del	NP_064632.2:n.853+251del
XM_005273201.1:c.853+251del	XP_005273258.1:n.853+251del
XM_011544238.1:c.853+251del	XP_011542540.1:n.853+251del
XM_011544239.1:c.853+251del	XP_011542541.1:n.853+251del
XM_011544240.1:c.853+251del	XP_011542542.1:n.853+251del
XM_011544241.1:c.853+251del	XP_011542543.1:n.853+251del
XM_011544239.2:c.853+251del	XP_011542541.1:n.853+251del
XM_011544241.2:c.853+251del	XP_011542543.1:n.853+251del
XM_017001852.1:c.853+251del	XP_016857341.1:n.853+251del
XM_024448517.1:c.853+251del	XP_024304285.1:n.853+251del
XM_024448518.1:c.853+251del	XP_024304286.1:n.853+251del
NM_020247.5:c.853+251del MANE Select	NP_064632.2:n.853+251del