Canonical Allele Identifier: CA3228902492

Gene: ACOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75949117C= , CM000679.2:g.75949117C=	GRCh38
NC_000017.10:g.73945198C= , CM000679.1:g.73945198C=	GRCh37
NC_000017.9:g.71456793C=	NCBI36
NG_008190.1:g.35247G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004035.7:c.1728+100G= MANE Select	NP_004026.2:n.1728+100G=
ENST00000293217.10:c.1728+100G= MANE Select	ENSP00000293217.4:n.1728+100G=
NM_001185039.1:c.1614+100G=	NP_001171968.1:n.1614+100G=
NM_001185039.2:c.1614+100G=	NP_001171968.1:n.1614+100G=
NM_004035.6:c.1728+100G=	NP_004026.2:n.1728+100G=
NM_007292.5:c.1728+100G=	NP_009223.2:n.1728+100G=
NM_007292.6:c.1728+100G=	NP_009223.2:n.1728+100G=
ENST00000293217.9:c.1728+100G=	ENSP00000293217.4:n.1728+100G=
ENST00000301608.8:c.1728+100G=	ENSP00000301608.4:n.1728+100G=
ENST00000301608.9:c.1728+100G=	ENSP00000301608.4:n.1728+100G=
ENST00000572047.5:c.1902+100G=	ENSP00000459936.1:n.1902+100G=
ENST00000573078.5:c.*1217+100G=	ENSP00000458325.1:n.*1217+100G=
ENST00000587927.5:c.143+100G=
ENST00000588968.5:c.182+100G=
XM_011524868.1:c.1524+100G=	XP_011523170.1:n.1524+100G=
XM_011524868.3:c.1524+100G=	XP_011523170.1:n.1524+100G=
XM_011524869.1:c.1320+100G=	XP_011523171.1:n.1320+100G=
XM_011524869.3:c.1320+100G=	XP_011523171.1:n.1320+100G=