Canonical Allele Identifier: CA1425246
Gene: COQ8A HGNC NCBI

Linked Data

dbSNP Id: rs765425276

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226982906A>G , CM000663.2:g.226982906A>G GRCh38
NC_000001.10:g.227170607A>G , CM000663.1:g.227170607A>G GRCh37
NC_000001.9:g.225237230A>G NCBI36
NG_012825.1:g.47670A>G
NG_012825.2:g.90371A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000366777.4:c.952A>G MANE Select ENSP00000355739.3:p.Asn318Asp
ENST00000366779.6:c.*5679A>G ENSP00000355741.2:n.*5679A>G
ENST00000676884.1:c.*5801A>G ENSP00000503200.1:n.*5801A>G
ENST00000366777.3:c.952A>G ENSP00000355739.3:p.Asn318Asp
ENST00000366778.5:c.796A>G ENSP00000355740.1:p.Asn266Asp
ENST00000366779.5:c.952A>G ENSP00000355741.1:p.Asn318Asp
ENST00000478406.5:n.931A>G
ENST00000485462.5:n.342A>G
NM_020247.4:c.952A>G NP_064632.2:p.Asn318Asp
XM_005273201.1:c.952A>G XP_005273258.1:p.Asn318Asp
XM_011544238.1:c.952A>G XP_011542540.1:p.Asn318Asp
XM_011544239.1:c.952A>G XP_011542541.1:p.Asn318Asp
XM_011544240.1:c.952A>G XP_011542542.1:p.Asn318Asp
XM_011544241.1:c.952A>G XP_011542543.1:p.Asn318Asp
XM_011544239.2:c.952A>G XP_011542541.1:p.Asn318Asp
XM_011544241.2:c.952A>G XP_011542543.1:p.Asn318Asp
XM_017001852.1:c.952A>G XP_016857341.1:p.Asn318Asp
XM_024448517.1:c.952A>G XP_024304285.1:p.Asn318Asp
XM_024448518.1:c.952A>G XP_024304286.1:p.Asn318Asp
NM_020247.5:c.952A>G MANE Select NP_064632.2:p.Asn318Asp