Canonical Allele Identifier: CA3894659

Gene: COX7A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75243727C>T , CM000668.2:g.75243727C>T	GRCh38
NC_000006.11:g.75953443C>T , CM000668.1:g.75953443C>T	GRCh37
NC_000006.10:g.76010163C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001366293.2:c.8G>A MANE Select	NP_001353222.1:p.Arg3Gln
ENST00000684430.2:c.8G>A MANE Select	ENSP00000506727.1:p.Arg3Gln
NM_001366292.1:c.104G>A	NP_001353221.1:p.Arg35Gln
NM_001366292.3:c.8G>A	NP_001353221.2:p.Arg3Gln
NM_001366293.1:c.8G>A	NP_001353222.1:p.Arg3Gln
NM_001865.3:c.104G>A	NP_001856.2:p.Arg35Gln
NM_001865.4:c.104G>A	NP_001856.2:p.Arg35Gln
NM_001865.6:c.8G>A	NP_001856.3:p.Arg3Gln
NR_029466.1:n.202G>A
NR_029466.2:n.523G>A
NR_158783.1:n.75G>A
NR_158784.1:n.75G>A
ENST00000370081.6:c.104G>A	ENSP00000359098.2:p.Arg35Gln
ENST00000370089.6:c.104G>A	ENSP00000359106.2:p.Arg35Gln
ENST00000377978.3:c.8G>A	ENSP00000421193.1:p.Arg3Gln
ENST00000459637.2:c.61G>A
ENST00000460985.1:c.8G>A	ENSP00000422979.1:p.Arg3Gln
ENST00000472311.6:c.8G>A	ENSP00000423432.1:p.Arg3Gln
ENST00000481061.2:n.83G>A
ENST00000509698.5:c.8G>A	ENSP00000425951.1:p.Arg3Gln
ENST00000509698.6:c.8G>A	ENSP00000425951.1:p.Arg3Gln
XM_011535445.1:c.104G>A	XP_011533747.1:p.Arg35Gln
XM_011535446.1:c.104G>A	XP_011533748.1:p.Arg35Gln
XM_024446330.1:c.104G>A	XP_024302098.1:p.Arg35Gln