Canonical Allele Identifier: CA401061591

Gene: ACOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75949898C>A , CM000679.2:g.75949898C>A	GRCh38
NC_000017.10:g.73945979C>A , CM000679.1:g.73945979C>A	GRCh37
NC_000017.9:g.71457574C>A	NCBI36
NG_008190.1:g.34466G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004035.7:c.1299-1G>T MANE Select	NP_004026.2:n.1299-1G>T
ENST00000293217.10:c.1299-1G>T MANE Select	ENSP00000293217.4:n.1299-1G>T
NM_001185039.1:c.1185-1G>T	NP_001171968.1:n.1185-1G>T
NM_001185039.2:c.1185-1G>T	NP_001171968.1:n.1185-1G>T
NM_004035.6:c.1299-1G>T	NP_004026.2:n.1299-1G>T
NM_007292.5:c.1299-1G>T	NP_009223.2:n.1299-1G>T
NM_007292.6:c.1299-1G>T	NP_009223.2:n.1299-1G>T
ENST00000293217.9:c.1299-1G>T	ENSP00000293217.4:n.1299-1G>T
ENST00000301608.8:c.1299-1G>T	ENSP00000301608.4:n.1299-1G>T
ENST00000301608.9:c.1299-1G>T	ENSP00000301608.4:n.1299-1G>T
ENST00000572047.5:c.1473-1G>T	ENSP00000459936.1:n.1473-1G>T
ENST00000573078.5:c.*788-1G>T	ENSP00000458325.1:n.*788-1G>T
XM_011524868.1:c.1095-1G>T	XP_011523170.1:n.1095-1G>T
XM_011524868.3:c.1095-1G>T	XP_011523170.1:n.1095-1G>T
XM_011524869.1:c.891-1G>T	XP_011523171.1:n.891-1G>T
XM_011524869.3:c.891-1G>T	XP_011523171.1:n.891-1G>T