Canonical Allele Identifier: CA2747999805
Gene: COQ8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226984802_226984803insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG , CM000663.2:g.226984802_226984803insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG GRCh38
NC_000001.10:g.227172503_227172504insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG , CM000663.1:g.227172503_227172504insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG GRCh37
NC_000001.9:g.225239126_225239127insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG NCBI36
NG_012825.1:g.49566_49567insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG
NG_012825.2:g.92267_92268insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000366777.4:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG MANE Select ENSP00000355739.3:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGG...
ENST00000366779.6:c.*6234-74_*6234-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG ENSP00000355741.2:n.*6234-74_*6234-73insAACAGTCCCTAGGGTAGGGTG...
ENST00000366777.3:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG ENSP00000355739.3:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGG...
ENST00000366778.5:c.1351-74_1351-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG ENSP00000355740.1:n.1351-74_1351-73insAACAGTCCCTAGGGTAGGGTGGG...
ENST00000366779.5:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG ENSP00000355741.1:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGG...
ENST00000478406.5:n.2369-74_2369-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG
ENST00000479852.1:n.694-74_694-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG
ENST00000485462.5:n.897-74_897-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG
NM_020247.4:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG NP_064632.2:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAAC...
XM_005273201.1:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG XP_005273258.1:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAA...
XM_011544238.1:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG XP_011542540.1:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAA...
XM_011544239.1:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG XP_011542541.1:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAA...
XM_011544240.1:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG XP_011542542.1:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAA...
XM_011544241.1:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG XP_011542543.1:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAA...
XM_011544239.2:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG XP_011542541.1:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAA...
XM_011544241.2:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG XP_011542543.1:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAA...
XM_017001852.1:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG XP_016857341.1:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAA...
XM_024448517.1:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG XP_024304285.1:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAA...
XM_024448518.1:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG XP_024304286.1:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAA...
NM_020247.5:c.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAACAGGAGGCAGGGG MANE Select NP_064632.2:n.1507-74_1507-73insAACAGTCCCTAGGGTAGGGTGGGTAAAAC...