Canonical Allele Identifier: CA1467986383

Gene: COX18

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73064835G= , CM000666.2:g.73064835G=	GRCh38
NC_000004.11:g.73930552G= , CM000666.1:g.73930552G=	GRCh37
NC_000004.10:g.74149416G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507544.3:c.666C= MANE Select	ENSP00000425261.3:p.Pro222=
ENST00000295890.8:c.663C=	ENSP00000295890.4:p.Pro221=
ENST00000449739.6:c.*172C=	ENSP00000394583.2:n.*172C=
ENST00000507544.2:c.666C=	ENSP00000425261.2:p.Pro222=
ENST00000510031.1:c.*283C=	ENSP00000424978.1:n.*283C=
NM_001297732.1:c.666C=	NP_001284661.1:p.Pro222=
NM_001297733.1:c.210C=	NP_001284662.1:p.Pro70=
NM_001300729.1:c.672C=	NP_001287658.1:p.Pro224=
NM_173827.3:c.663C=	NP_776188.1:p.Pro221=
XM_005265680.3:c.666C=	XP_005265737.1:p.Pro222=
XM_011531878.1:c.213C=	XP_011530180.1:p.Pro71=
XM_005265680.5:c.666C=	XP_005265737.1:p.Pro222=
XM_011531878.3:c.213C=	XP_011530180.1:p.Pro71=
XM_017008045.2:c.663C=	XP_016863534.1:p.Pro221=
XR_001741209.2:n.759C=
XR_002959725.1:n.1964C=
NM_001297732.2:c.666C= MANE Select	NP_001284661.1:p.Pro222=
NM_001297733.2:c.210C=	NP_001284662.1:p.Pro70=
NM_173827.4:c.663C=	NP_776188.1:p.Pro221=