Canonical Allele Identifier: CA345053200

Gene: COQ8A

Linked Data

• gnomAD v4: 1-226983025-G-T
• MyVariant Identifiers: chr1:g.227170726G>T (hg19) ; chr1:g.226983025G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226983025G>T , CM000663.2:g.226983025G>T	GRCh38
NC_000001.10:g.227170726G>T , CM000663.1:g.227170726G>T	GRCh37
NC_000001.9:g.225237349G>T	NCBI36
NG_012825.1:g.47789G>T
NG_012825.2:g.90490G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.1071G>T MANE Select	ENSP00000355739.3:p.Met357Ile
ENST00000366779.6:c.*5798G>T	ENSP00000355741.2:n.*5798G>T
ENST00000676884.1:c.*5920G>T	ENSP00000503200.1:n.*5920G>T
ENST00000366777.3:c.1071G>T	ENSP00000355739.3:p.Met357Ile
ENST00000366778.5:c.915G>T	ENSP00000355740.1:p.Met305Ile
ENST00000366779.5:c.1071G>T	ENSP00000355741.1:p.Met357Ile
ENST00000478406.5:n.1050G>T
ENST00000479852.1:n.19G>T
ENST00000485462.5:n.461G>T
NM_020247.4:c.1071G>T	NP_064632.2:p.Met357Ile
XM_005273201.1:c.1071G>T	XP_005273258.1:p.Met357Ile
XM_011544238.1:c.1071G>T	XP_011542540.1:p.Met357Ile
XM_011544239.1:c.1071G>T	XP_011542541.1:p.Met357Ile
XM_011544240.1:c.1071G>T	XP_011542542.1:p.Met357Ile
XM_011544241.1:c.1071G>T	XP_011542543.1:p.Met357Ile
XM_011544239.2:c.1071G>T	XP_011542541.1:p.Met357Ile
XM_011544241.2:c.1071G>T	XP_011542543.1:p.Met357Ile
XM_017001852.1:c.1071G>T	XP_016857341.1:p.Met357Ile
XM_024448517.1:c.1071G>T	XP_024304285.1:p.Met357Ile
XM_024448518.1:c.1071G>T	XP_024304286.1:p.Met357Ile
NM_020247.5:c.1071G>T MANE Select	NP_064632.2:p.Met357Ile