Canonical Allele Identifier: CA2275766774

Gene: ACOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75960240A= , CM000679.2:g.75960240A=	GRCh38
NC_000017.10:g.73956321A= , CM000679.1:g.73956321A=	GRCh37
NC_000017.9:g.71467916A=	NCBI36
NG_008190.1:g.24124T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301608.9:c.431-2674T=	ENSP00000301608.4:n.431-2674T=
ENST00000293217.10:c.405T= MANE Select	ENSP00000293217.4:p.Thr135=
ENST00000293217.9:c.405T=	ENSP00000293217.4:p.Thr135=
ENST00000301608.8:c.431-2674T=	ENSP00000301608.4:n.431-2674T=
ENST00000572047.5:c.579T=	ENSP00000459936.1:n.579T=
ENST00000573078.5:c.566T=	ENSP00000458325.1:p.Leu189=
ENST00000588176.5:c.431-4293T=	ENSP00000466210.1:n.431-4293T=
ENST00000589301.1:c.*228-2674T=	ENSP00000468435.1:n.*228-2674T=
ENST00000591857.5:n.423T=
NM_001185039.1:c.291T=	NP_001171968.1:p.Thr97=
NM_004035.6:c.405T=	NP_004026.2:p.Thr135=
NM_007292.5:c.431-2674T=	NP_009223.2:n.431-2674T=
XM_011524868.1:c.201T=	XP_011523170.1:p.Thr67=
XM_011524869.1:c.23-2674T=	XP_011523171.1:n.23-2674T=
XM_011524868.3:c.201T=	XP_011523170.1:p.Thr67=
XM_011524869.3:c.23-2674T=	XP_011523171.1:n.23-2674T=
NM_004035.7:c.405T= MANE Select	NP_004026.2:p.Thr135=
NM_001185039.2:c.291T=	NP_001171968.1:p.Thr97=
NM_007292.6:c.431-2674T=	NP_009223.2:n.431-2674T=