Canonical Allele Identifier: CA2639926484

Gene: ACOX1

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75960140A>C , CM000679.2:g.75960140A>C	GRCh38
NC_000017.10:g.73956221A>C , CM000679.1:g.73956221A>C	GRCh37
NC_000017.9:g.71467816A>C	NCBI36
NG_008190.1:g.24224T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301608.9:c.431-2574T>G	ENSP00000301608.4:n.431-2574T>G
ENST00000293217.10:c.430+75T>G MANE Select	ENSP00000293217.4:n.430+75T>G
ENST00000293217.9:c.430+75T>G	ENSP00000293217.4:n.430+75T>G
ENST00000301608.8:c.431-2574T>G	ENSP00000301608.4:n.431-2574T>G
ENST00000572047.5:c.604+75T>G	ENSP00000459936.1:n.604+75T>G
ENST00000573078.5:c.591+75T>G	ENSP00000458325.1:n.591+75T>G
ENST00000588176.5:c.431-4193T>G	ENSP00000466210.1:n.431-4193T>G
ENST00000589301.1:c.*228-2574T>G	ENSP00000468435.1:n.*228-2574T>G
ENST00000591857.5:n.448+75T>G
NM_001185039.1:c.316+75T>G	NP_001171968.1:n.316+75T>G
NM_004035.6:c.430+75T>G	NP_004026.2:n.430+75T>G
NM_007292.5:c.431-2574T>G	NP_009223.2:n.431-2574T>G
XM_011524868.1:c.226+75T>G	XP_011523170.1:n.226+75T>G
XM_011524869.1:c.23-2574T>G	XP_011523171.1:n.23-2574T>G
XM_011524868.3:c.226+75T>G	XP_011523170.1:n.226+75T>G
XM_011524869.3:c.23-2574T>G	XP_011523171.1:n.23-2574T>G
NM_004035.7:c.430+75T>G MANE Select	NP_004026.2:n.430+75T>G
NM_001185039.2:c.316+75T>G	NP_001171968.1:n.316+75T>G
NM_007292.6:c.431-2574T>G	NP_009223.2:n.431-2574T>G