Canonical Allele Identifier: CA353373186

Gene: ACOX2

Linked Data

• MyVariant Identifiers: chr3:g.58520203A>C (hg19) ; chr3:g.58534476A>C (hg38)

Genomic Alleles

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

Transcript Alleles

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