Canonical Allele Identifier: CA16044013
Gene: ACOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 375219
ClinVar RCV Id: RCV000416307
dbSNP Id: rs1057519329

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.58534476A>T , CM000665.2:g.58534476A>T GRCh38
NC_000003.11:g.58520203A>T , CM000665.1:g.58520203A>T GRCh37
NC_000003.10:g.58495243A>T NCBI36
NG_052668.1:g.7727T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000302819.10:c.207T>A MANE Select ENSP00000307697.5:p.Tyr69Ter
ENST00000302819.9:c.207T>A ENSP00000307697.5:p.Tyr69Ter
ENST00000459701.6:c.207T>A ENSP00000418562.2:p.Tyr69Ter
ENST00000466689.1:n.441T>A
ENST00000474098.1:c.207T>A ENSP00000419927.1:p.Tyr69Ter
ENST00000475143.5:n.338+100T>A
ENST00000492530.1:c.152+14T>A
NM_003500.3:c.207T>A NP_003491.1:p.Tyr69Ter
XM_005265505.1:c.207T>A XP_005265562.1:p.Tyr69Ter
XM_005265506.2:c.-4T>A XP_005265563.1:n.-4T>A
XM_006713340.2:c.29+100T>A XP_006713403.1:n.29+100T>A
XM_011534147.1:c.372T>A XP_011532449.1:p.Tyr124Ter
XM_011534148.1:c.29+100T>A XP_011532450.1:n.29+100T>A
XM_006713340.3:c.29+100T>A XP_006713403.1:n.29+100T>A
XM_017007302.2:c.-4T>A XP_016862791.1:n.-4T>A
XM_024453786.1:c.-4T>A XP_024309554.1:n.-4T>A
NM_003500.4:c.207T>A MANE Select NP_003491.1:p.Tyr69Ter