Canonical Allele Identifier: CA1012968978
Gene: COQ8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226984863_226984878dup , CM000663.2:g.226984863_226984878dup GRCh38
NC_000001.10:g.227172564_227172579dup , CM000663.1:g.227172564_227172579dup GRCh37
NC_000001.9:g.225239187_225239202dup NCBI36
NG_012825.1:g.49627_49642dup
NG_012825.2:g.92328_92343dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000366777.4:c.1507-13_1509dup
ENST00000366779.6:c.*6234-13_*6236dup
ENST00000366777.3:c.1507-13_1509dup
ENST00000366778.5:c.1351-13_1353dup
ENST00000366779.5:c.1507-13_1509dup
ENST00000478406.5:n.2369-13_2371dup
ENST00000479852.1:n.694-13_696dup
ENST00000485462.5:n.897-13_899dup
NM_020247.4:c.1507-13_1509dup
XM_005273201.1:c.1507-13_1509dup
XM_011544238.1:c.1507-13_1509dup
XM_011544239.1:c.1507-13_1509dup
XM_011544240.1:c.1507-13_1509dup
XM_011544241.1:c.1507-13_1509dup
XM_011544239.2:c.1507-13_1509dup
XM_011544241.2:c.1507-13_1509dup
XM_017001852.1:c.1507-13_1509dup
XM_024448517.1:c.1507-13_1509dup
XM_024448518.1:c.1507-13_1509dup
NM_020247.5:c.1507-13_1509dup