Canonical Allele Identifier: CA2851238

Gene: ACOX3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.8389631G>A , CM000666.2:g.8389631G>A	GRCh38
NC_000004.11:g.8391358G>A , CM000666.1:g.8391358G>A	GRCh37
NC_000004.10:g.8442258G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356406.10:c.1404C>T MANE Select	ENSP00000348775.4:p.Leu468=
ENST00000356406.9:c.1404C>T	ENSP00000348775.4:p.Leu468=
ENST00000413009.6:c.1404C>T	ENSP00000413994.2:p.Leu468=
ENST00000503233.5:c.1404C>T	ENSP00000421625.1:p.Leu468=
ENST00000508302.1:n.389C>T
ENST00000510365.5:n.1116C>T
NM_001101667.1:c.1404C>T	NP_001095137.1:p.Leu468=
NM_003501.2:c.1404C>T	NP_003492.2:p.Leu468=
XM_005248011.3:c.1404C>T	XP_005248068.1:p.Leu468=
XM_005248012.3:c.1404C>T	XP_005248069.1:p.Leu468=
XM_005248013.3:c.1404C>T	XP_005248070.1:p.Leu468=
XM_011513565.1:c.1404C>T	XP_011511867.1:p.Leu468=
XM_011513566.1:c.1404C>T	XP_011511868.1:p.Leu468=
XM_011513567.1:c.1404C>T	XP_011511869.1:p.Leu468=
XR_925000.1:n.1549C>T
XM_005248011.4:c.1404C>T	XP_005248068.1:p.Leu468=
XM_011513565.2:c.1404C>T	XP_011511867.1:p.Leu468=
XM_024454237.1:c.1404C>T	XP_024310005.1:p.Leu468=
NM_003501.3:c.1404C>T MANE Select	NP_003492.2:p.Leu468=
NM_001101667.2:c.1404C>T	NP_001095137.1:p.Leu468=
NM_001375783.1:c.1404C>T	NP_001362712.1:p.Leu468=
NM_001375784.1:c.1332C>T	NP_001362713.1:p.Leu444=
NM_001375785.1:c.1404C>T	NP_001362714.1:p.Leu468=
NM_001375786.1:c.1404C>T	NP_001362715.1:p.Leu468=
NM_001375787.1:c.1404C>T	NP_001362716.1:p.Leu468=
NM_001375788.1:c.1404C>T	NP_001362717.1:p.Leu468=
NM_001375789.1:c.1119C>T	NP_001362718.1:p.Leu373=
NM_001375790.1:c.1404C>T	NP_001362719.1:p.Leu468=