Canonical Allele Identifier: CA2275763247

Gene: ACOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75953479C= , CM000679.2:g.75953479C=	GRCh38
NC_000017.10:g.73949560C= , CM000679.1:g.73949560C=	GRCh37
NC_000017.9:g.71461155C=	NCBI36
NG_008190.1:g.30885G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301608.9:c.916G=	ENSP00000301608.4:p.Val306=
ENST00000293217.10:c.916G= MANE Select	ENSP00000293217.4:p.Val306=
ENST00000293217.9:c.916G=	ENSP00000293217.4:p.Val306=
ENST00000301608.8:c.916G=	ENSP00000301608.4:p.Val306=
ENST00000572047.5:c.1090G=	ENSP00000459936.1:n.1090G=
ENST00000573078.5:c.*405G=	ENSP00000458325.1:n.*405G=
ENST00000589744.1:n.166G=
NM_001185039.1:c.802G=	NP_001171968.1:p.Val268=
NM_004035.6:c.916G=	NP_004026.2:p.Val306=
NM_007292.5:c.916G=	NP_009223.2:p.Val306=
XM_011524868.1:c.712G=	XP_011523170.1:p.Val238=
XM_011524869.1:c.508G=	XP_011523171.1:p.Val170=
XM_011524868.3:c.712G=	XP_011523170.1:p.Val238=
XM_011524869.3:c.508G=	XP_011523171.1:p.Val170=
NM_004035.7:c.916G= MANE Select	NP_004026.2:p.Val306=
NM_001185039.2:c.802G=	NP_001171968.1:p.Val268=
NM_007292.6:c.916G=	NP_009223.2:p.Val306=