Canonical Allele Identifier: CA2838443761

Gene: ACOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75949122A>T , CM000679.2:g.75949122A>T	GRCh38
NC_000017.10:g.73945203A>T , CM000679.1:g.73945203A>T	GRCh37
NC_000017.9:g.71456798A>T	NCBI36
NG_008190.1:g.35242T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004035.7:c.1728+95T>A MANE Select	NP_004026.2:n.1728+95T>A
ENST00000293217.10:c.1728+95T>A MANE Select	ENSP00000293217.4:n.1728+95T>A
NM_001185039.1:c.1614+95T>A	NP_001171968.1:n.1614+95T>A
NM_001185039.2:c.1614+95T>A	NP_001171968.1:n.1614+95T>A
NM_004035.6:c.1728+95T>A	NP_004026.2:n.1728+95T>A
NM_007292.5:c.1728+95T>A	NP_009223.2:n.1728+95T>A
NM_007292.6:c.1728+95T>A	NP_009223.2:n.1728+95T>A
ENST00000293217.9:c.1728+95T>A	ENSP00000293217.4:n.1728+95T>A
ENST00000301608.8:c.1728+95T>A	ENSP00000301608.4:n.1728+95T>A
ENST00000301608.9:c.1728+95T>A	ENSP00000301608.4:n.1728+95T>A
ENST00000572047.5:c.1902+95T>A	ENSP00000459936.1:n.1902+95T>A
ENST00000573078.5:c.*1217+95T>A	ENSP00000458325.1:n.*1217+95T>A
ENST00000587927.5:c.143+95T>A
ENST00000588968.5:c.182+95T>A
XM_011524868.1:c.1524+95T>A	XP_011523170.1:n.1524+95T>A
XM_011524868.3:c.1524+95T>A	XP_011523170.1:n.1524+95T>A
XM_011524869.1:c.1320+95T>A	XP_011523171.1:n.1320+95T>A
XM_011524869.3:c.1320+95T>A	XP_011523171.1:n.1320+95T>A