Canonical Allele Identifier: CA2275763243

Gene: ACOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75953469T= , CM000679.2:g.75953469T=	GRCh38
NC_000017.10:g.73949550T= , CM000679.1:g.73949550T=	GRCh37
NC_000017.9:g.71461145T=	NCBI36
NG_008190.1:g.30895A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301608.9:c.926A=	ENSP00000301608.4:p.Gln309=
ENST00000293217.10:c.926A= MANE Select	ENSP00000293217.4:p.Gln309=
ENST00000293217.9:c.926A=	ENSP00000293217.4:p.Gln309=
ENST00000301608.8:c.926A=	ENSP00000301608.4:p.Gln309=
ENST00000572047.5:c.1100A=	ENSP00000459936.1:n.1100A=
ENST00000573078.5:c.*415A=	ENSP00000458325.1:n.*415A=
ENST00000589744.1:n.176A=
NM_001185039.1:c.812A=	NP_001171968.1:p.Gln271=
NM_004035.6:c.926A=	NP_004026.2:p.Gln309=
NM_007292.5:c.926A=	NP_009223.2:p.Gln309=
XM_011524868.1:c.722A=	XP_011523170.1:p.Gln241=
XM_011524869.1:c.518A=	XP_011523171.1:p.Gln173=
XM_011524868.3:c.722A=	XP_011523170.1:p.Gln241=
XM_011524869.3:c.518A=	XP_011523171.1:p.Gln173=
NM_004035.7:c.926A= MANE Select	NP_004026.2:p.Gln309=
NM_001185039.2:c.812A=	NP_001171968.1:p.Gln271=
NM_007292.6:c.926A=	NP_009223.2:p.Gln309=