Canonical Allele Identifier: CA356241821
Gene: ACOX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.8381571A>G , CM000666.2:g.8381571A>G GRCh38
NC_000004.11:g.8383298A>G , CM000666.1:g.8383298A>G GRCh37
NC_000004.10:g.8434198A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356406.10:c.1574T>C MANE Select ENSP00000348775.4:p.Leu525Pro
ENST00000356406.9:c.1574T>C ENSP00000348775.4:p.Leu525Pro
ENST00000413009.6:c.1574T>C ENSP00000413994.2:p.Leu525Pro
ENST00000503233.5:c.1574T>C ENSP00000421625.1:p.Leu525Pro
ENST00000508302.1:n.559T>C
ENST00000510365.5:n.1286T>C
NM_001101667.1:c.1574T>C NP_001095137.1:p.Leu525Pro
NM_003501.2:c.1574T>C NP_003492.2:p.Leu525Pro
XM_005248011.3:c.1574T>C XP_005248068.1:p.Leu525Pro
XM_005248012.3:c.1574T>C XP_005248069.1:p.Leu525Pro
XM_005248013.3:c.1574T>C XP_005248070.1:p.Leu525Pro
XM_011513565.1:c.1574T>C XP_011511867.1:p.Leu525Pro
XM_011513566.1:c.1574T>C XP_011511868.1:p.Leu525Pro
XR_925000.1:n.1719T>C
XM_005248011.4:c.1574T>C XP_005248068.1:p.Leu525Pro
XM_011513565.2:c.1574T>C XP_011511867.1:p.Leu525Pro
NM_003501.3:c.1574T>C MANE Select NP_003492.2:p.Leu525Pro
NM_001101667.2:c.1574T>C NP_001095137.1:p.Leu525Pro
NM_001375783.1:c.1574T>C NP_001362712.1:p.Leu525Pro
NM_001375784.1:c.1502T>C NP_001362713.1:p.Leu501Pro
NM_001375785.1:c.1574T>C NP_001362714.1:p.Leu525Pro
NM_001375786.1:c.1574T>C NP_001362715.1:p.Leu525Pro
NM_001375787.1:c.1574T>C NP_001362716.1:p.Leu525Pro
NM_001375788.1:c.1574T>C NP_001362717.1:p.Leu525Pro
NM_001375789.1:c.1289T>C NP_001362718.1:p.Leu430Pro
NM_001375790.1:c.1574T>C NP_001362719.1:p.Leu525Pro