Canonical Allele Identifier: CA2275766775

Gene: ACOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75960243G= , CM000679.2:g.75960243G=	GRCh38
NC_000017.10:g.73956324G= , CM000679.1:g.73956324G=	GRCh37
NC_000017.9:g.71467919G=	NCBI36
NG_008190.1:g.24121C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301608.9:c.431-2677C=	ENSP00000301608.4:n.431-2677C=
ENST00000293217.10:c.402C= MANE Select	ENSP00000293217.4:p.Gly134=
ENST00000293217.9:c.402C=	ENSP00000293217.4:p.Gly134=
ENST00000301608.8:c.431-2677C=	ENSP00000301608.4:n.431-2677C=
ENST00000572047.5:c.576C=	ENSP00000459936.1:n.576C=
ENST00000573078.5:c.563C=	ENSP00000458325.1:p.Ala188=
ENST00000588176.5:c.431-4296C=	ENSP00000466210.1:n.431-4296C=
ENST00000589301.1:c.*228-2677C=	ENSP00000468435.1:n.*228-2677C=
ENST00000591857.5:n.420C=
NM_001185039.1:c.288C=	NP_001171968.1:p.Gly96=
NM_004035.6:c.402C=	NP_004026.2:p.Gly134=
NM_007292.5:c.431-2677C=	NP_009223.2:n.431-2677C=
XM_011524868.1:c.198C=	XP_011523170.1:p.Gly66=
XM_011524869.1:c.23-2677C=	XP_011523171.1:n.23-2677C=
XM_011524868.3:c.198C=	XP_011523170.1:p.Gly66=
XM_011524869.3:c.23-2677C=	XP_011523171.1:n.23-2677C=
NM_004035.7:c.402C= MANE Select	NP_004026.2:p.Gly134=
NM_001185039.2:c.288C=	NP_001171968.1:p.Gly96=
NM_007292.6:c.431-2677C=	NP_009223.2:n.431-2677C=