Canonical Allele Identifier: CA2275763245

Gene: ACOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75953471G= , CM000679.2:g.75953471G=	GRCh38
NC_000017.10:g.73949552G= , CM000679.1:g.73949552G=	GRCh37
NC_000017.9:g.71461147G=	NCBI36
NG_008190.1:g.30893C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301608.9:c.924C=	ENSP00000301608.4:p.His308=
ENST00000293217.10:c.924C= MANE Select	ENSP00000293217.4:p.His308=
ENST00000293217.9:c.924C=	ENSP00000293217.4:p.His308=
ENST00000301608.8:c.924C=	ENSP00000301608.4:p.His308=
ENST00000572047.5:c.1098C=	ENSP00000459936.1:n.1098C=
ENST00000573078.5:c.*413C=	ENSP00000458325.1:n.*413C=
ENST00000589744.1:n.174C=
NM_001185039.1:c.810C=	NP_001171968.1:p.His270=
NM_004035.6:c.924C=	NP_004026.2:p.His308=
NM_007292.5:c.924C=	NP_009223.2:p.His308=
XM_011524868.1:c.720C=	XP_011523170.1:p.His240=
XM_011524869.1:c.516C=	XP_011523171.1:p.His172=
XM_011524868.3:c.720C=	XP_011523170.1:p.His240=
XM_011524869.3:c.516C=	XP_011523171.1:p.His172=
NM_004035.7:c.924C= MANE Select	NP_004026.2:p.His308=
NM_001185039.2:c.810C=	NP_001171968.1:p.His270=
NM_007292.6:c.924C=	NP_009223.2:p.His308=