Canonical Allele Identifier: CA8776913

Gene: ACOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75953599C>T , CM000679.2:g.75953599C>T	GRCh38
NC_000017.10:g.73949680C>T , CM000679.1:g.73949680C>T	GRCh37
NC_000017.9:g.71461275C>T	NCBI36
NG_008190.1:g.30765G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004035.7:c.796G>A MANE Select	NP_004026.2:p.Val266Met
ENST00000293217.10:c.796G>A MANE Select	ENSP00000293217.4:p.Val266Met
NM_001185039.1:c.682G>A	NP_001171968.1:p.Val228Met
NM_001185039.2:c.682G>A	NP_001171968.1:p.Val228Met
NM_004035.6:c.796G>A	NP_004026.2:p.Val266Met
NM_007292.5:c.796G>A	NP_009223.2:p.Val266Met
NM_007292.6:c.796G>A	NP_009223.2:p.Val266Met
ENST00000293217.9:c.796G>A	ENSP00000293217.4:p.Val266Met
ENST00000301608.8:c.796G>A	ENSP00000301608.4:p.Val266Met
ENST00000301608.9:c.796G>A	ENSP00000301608.4:p.Val266Met
ENST00000572047.5:c.970G>A	ENSP00000459936.1:n.970G>A
ENST00000573078.5:c.*285G>A	ENSP00000458325.1:n.*285G>A
ENST00000589744.1:n.46G>A
XM_011524868.1:c.592G>A	XP_011523170.1:p.Val198Met
XM_011524868.3:c.592G>A	XP_011523170.1:p.Val198Met
XM_011524869.1:c.388G>A	XP_011523171.1:p.Val130Met
XM_011524869.3:c.388G>A	XP_011523171.1:p.Val130Met