Canonical Allele Identifier: CA1225124392

Gene: COQ8A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226984651_226984674delinsACAAGGTGAGCCCCAGGGTGGGGG , CM000663.2:g.226984651_226984674delinsACAAGGTGAGCCCCAGGGTGGGGG	GRCh38
NC_000001.10:g.227172352_227172375delinsACAAGGTGAGCCCCAGGGTGGGGG , CM000663.1:g.227172352_227172375delinsACAAGGTGAGCCCCAGGGTGGGGG	GRCh37
NC_000001.9:g.225238975_225238998delinsACAAGGTGAGCCCCAGGGTGGGGG	NCBI36
NG_012825.1:g.49415_49438delinsACAAGGTGAGCCCCAGGGTGGGGG
NG_012825.2:g.92116_92139delinsACAAGGTGAGCCCCAGGGTGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG
ENST00000366779.6:c.*6229_*6233+19delinsACAAGGTGAGCCCCAGGGTGGGGG
ENST00000366777.3:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG
ENST00000366778.5:c.1346_1350+19delinsACAAGGTGAGCCCCAGGGTGGGGG
ENST00000366779.5:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG
ENST00000478406.5:n.2364_2368+19delinsACAAGGTGAGCCCCAGGGTGGGGG
ENST00000479852.1:n.689_693+19delinsACAAGGTGAGCCCCAGGGTGGGGG
ENST00000485462.5:n.892_896+19delinsACAAGGTGAGCCCCAGGGTGGGGG
NM_020247.4:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG
XM_005273201.1:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG
XM_011544238.1:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG
XM_011544239.1:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG
XM_011544240.1:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG
XM_011544241.1:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG
XM_011544239.2:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG
XM_011544241.2:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG
XM_017001852.1:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG
XM_024448517.1:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG
XM_024448518.1:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG
NM_020247.5:c.1502_1506+19delinsACAAGGTGAGCCCCAGGGTGGGGG