Canonical Allele Identifier: CA2275766777

Gene: ACOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75960249G= , CM000679.2:g.75960249G=	GRCh38
NC_000017.10:g.73956330G= , CM000679.1:g.73956330G=	GRCh37
NC_000017.9:g.71467925G=	NCBI36
NG_008190.1:g.24115C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301608.9:c.431-2683C=	ENSP00000301608.4:n.431-2683C=
ENST00000293217.10:c.396C= MANE Select	ENSP00000293217.4:p.Ile132=
ENST00000293217.9:c.396C=	ENSP00000293217.4:p.Ile132=
ENST00000301608.8:c.431-2683C=	ENSP00000301608.4:n.431-2683C=
ENST00000572047.5:c.570C=	ENSP00000459936.1:n.570C=
ENST00000573078.5:c.557C=	ENSP00000458325.1:p.Ser186=
ENST00000588176.5:c.431-4302C=	ENSP00000466210.1:n.431-4302C=
ENST00000589301.1:c.*228-2683C=	ENSP00000468435.1:n.*228-2683C=
ENST00000591857.5:n.414C=
NM_001185039.1:c.282C=	NP_001171968.1:p.Ile94=
NM_004035.6:c.396C=	NP_004026.2:p.Ile132=
NM_007292.5:c.431-2683C=	NP_009223.2:n.431-2683C=
XM_011524868.1:c.192C=	XP_011523170.1:p.Ile64=
XM_011524869.1:c.23-2683C=	XP_011523171.1:n.23-2683C=
XM_011524868.3:c.192C=	XP_011523170.1:p.Ile64=
XM_011524869.3:c.23-2683C=	XP_011523171.1:n.23-2683C=
NM_004035.7:c.396C= MANE Select	NP_004026.2:p.Ile132=
NM_001185039.2:c.282C=	NP_001171968.1:p.Ile94=
NM_007292.6:c.431-2683C=	NP_009223.2:n.431-2683C=