Canonical Allele Identifier: CA151597

Gene: COQ8A

Linked Data

• ClinVar Variation Id: 128274
• ClinVar RCV Id: RCV000116235 ; RCV000373810 ; RCV000614204 ; RCV000676181
• dbSNP Id: rs12593
• ExAC: 1:227172290 C / T
• gnomAD v2: 1-227172290-C-T
• gnomAD v3: 1-226984589-C-T
• gnomAD v4: 1-226984589-C-T
• MyVariant Identifiers: chr1:g.227172290C>T (hg19) ; chr1:g.226984589C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226984589C>T , CM000663.2:g.226984589C>T	GRCh38
NC_000001.10:g.227172290C>T , CM000663.1:g.227172290C>T	GRCh37
NC_000001.9:g.225238913C>T	NCBI36
NG_012825.1:g.49353C>T
NG_012825.2:g.92054C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.1440C>T MANE Select	ENSP00000355739.3:p.Phe480=
ENST00000366779.6:c.*6167C>T	ENSP00000355741.2:n.*6167C>T
ENST00000366777.3:c.1440C>T	ENSP00000355739.3:p.Phe480=
ENST00000366778.5:c.1284C>T	ENSP00000355740.1:p.Phe428=
ENST00000366779.5:c.1440C>T	ENSP00000355741.1:p.Phe480=
ENST00000478406.5:n.2302C>T
ENST00000479852.1:n.627C>T
ENST00000485462.5:n.830C>T
NM_020247.4:c.1440C>T	NP_064632.2:p.Phe480=
XM_005273201.1:c.1440C>T	XP_005273258.1:p.Phe480=
XM_011544238.1:c.1440C>T	XP_011542540.1:p.Phe480=
XM_011544239.1:c.1440C>T	XP_011542541.1:p.Phe480=
XM_011544240.1:c.1440C>T	XP_011542542.1:p.Phe480=
XM_011544241.1:c.1440C>T	XP_011542543.1:p.Phe480=
XM_011544239.2:c.1440C>T	XP_011542541.1:p.Phe480=
XM_011544241.2:c.1440C>T	XP_011542543.1:p.Phe480=
XM_017001852.1:c.1440C>T	XP_016857341.1:p.Phe480=
XM_024448517.1:c.1440C>T	XP_024304285.1:p.Phe480=
XM_024448518.1:c.1440C>T	XP_024304286.1:p.Phe480=
NM_020247.5:c.1440C>T MANE Select	NP_064632.2:p.Phe480=