Canonical Allele Identifier: CA38645414

Gene: COQ8A

Linked Data

• dbSNP Id: rs55798516
• gnomAD v3: 1-226982976-T-C
• gnomAD v4: 1-226982976-T-C
• MyVariant Identifiers: chr1:g.227170677T>C (hg19) ; chr1:g.226982976T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226982976T>C , CM000663.2:g.226982976T>C	GRCh38
NC_000001.10:g.227170677T>C , CM000663.1:g.227170677T>C	GRCh37
NC_000001.9:g.225237300T>C	NCBI36
NG_012825.1:g.47740T>C
NG_012825.2:g.90441T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.1022T>C MANE Select	ENSP00000355739.3:p.Ile341Thr
ENST00000366779.6:c.*5749T>C	ENSP00000355741.2:n.*5749T>C
ENST00000676884.1:c.*5871T>C	ENSP00000503200.1:n.*5871T>C
ENST00000366777.3:c.1022T>C	ENSP00000355739.3:p.Ile341Thr
ENST00000366778.5:c.866T>C	ENSP00000355740.1:p.Ile289Thr
ENST00000366779.5:c.1022T>C	ENSP00000355741.1:p.Ile341Thr
ENST00000478406.5:n.1001T>C
ENST00000485462.5:n.412T>C
NM_020247.4:c.1022T>C	NP_064632.2:p.Ile341Thr
XM_005273201.1:c.1022T>C	XP_005273258.1:p.Ile341Thr
XM_011544238.1:c.1022T>C	XP_011542540.1:p.Ile341Thr
XM_011544239.1:c.1022T>C	XP_011542541.1:p.Ile341Thr
XM_011544240.1:c.1022T>C	XP_011542542.1:p.Ile341Thr
XM_011544241.1:c.1022T>C	XP_011542543.1:p.Ile341Thr
XM_011544239.2:c.1022T>C	XP_011542541.1:p.Ile341Thr
XM_011544241.2:c.1022T>C	XP_011542543.1:p.Ile341Thr
XM_017001852.1:c.1022T>C	XP_016857341.1:p.Ile341Thr
XM_024448517.1:c.1022T>C	XP_024304285.1:p.Ile341Thr
XM_024448518.1:c.1022T>C	XP_024304286.1:p.Ile341Thr
NM_020247.5:c.1022T>C MANE Select	NP_064632.2:p.Ile341Thr