Canonical Allele Identifier: CA8777060

Gene: ACOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75960383G>C , CM000679.2:g.75960383G>C	GRCh38
NC_000017.10:g.73956464G>C , CM000679.1:g.73956464G>C	GRCh37
NC_000017.9:g.71468059G>C	NCBI36
NG_008190.1:g.23981C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004035.7:c.270-8C>G MANE Select	NP_004026.2:n.270-8C>G
ENST00000293217.10:c.270-8C>G MANE Select	ENSP00000293217.4:n.270-8C>G
NM_001185039.1:c.156-8C>G	NP_001171968.1:n.156-8C>G
NM_001185039.2:c.156-8C>G	NP_001171968.1:n.156-8C>G
NM_004035.6:c.270-8C>G	NP_004026.2:n.270-8C>G
NM_007292.5:c.431-2817C>G	NP_009223.2:n.431-2817C>G
NM_007292.6:c.431-2817C>G	NP_009223.2:n.431-2817C>G
ENST00000293217.9:c.270-8C>G	ENSP00000293217.4:n.270-8C>G
ENST00000301608.8:c.431-2817C>G	ENSP00000301608.4:n.431-2817C>G
ENST00000301608.9:c.431-2817C>G	ENSP00000301608.4:n.431-2817C>G
ENST00000572047.5:c.444-8C>G	ENSP00000459936.1:n.444-8C>G
ENST00000573078.5:c.431-8C>G	ENSP00000458325.1:n.431-8C>G
ENST00000588176.5:c.431-4436C>G	ENSP00000466210.1:n.431-4436C>G
ENST00000589301.1:c.*228-2817C>G	ENSP00000468435.1:n.*228-2817C>G
ENST00000591857.5:n.288-8C>G
XM_011524868.1:c.66-8C>G	XP_011523170.1:n.66-8C>G
XM_011524868.3:c.66-8C>G	XP_011523170.1:n.66-8C>G
XM_011524869.1:c.23-2817C>G	XP_011523171.1:n.23-2817C>G
XM_011524869.3:c.23-2817C>G	XP_011523171.1:n.23-2817C>G