Canonical Allele Identifier: CA2472566

Gene: ACOX2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58535132A>G , CM000665.2:g.58535132A>G	GRCh38
NC_000003.11:g.58520859A>G , CM000665.1:g.58520859A>G	GRCh37
NC_000003.10:g.58495899A>G	NCBI36
NG_052668.1:g.7071T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003500.4:c.-26T>C MANE Select	NP_003491.1:n.-26T>C
ENST00000302819.10:c.-26T>C MANE Select	ENSP00000307697.5:n.-26T>C
NM_003500.3:c.-26T>C	NP_003491.1:n.-26T>C
ENST00000302819.9:c.-26T>C	ENSP00000307697.5:n.-26T>C
ENST00000459701.6:c.-26T>C	ENSP00000418562.2:n.-26T>C
ENST00000466689.1:n.123T>C
ENST00000474098.1:c.-26T>C	ENSP00000419927.1:n.-26T>C
ENST00000475143.5:n.120T>C
ENST00000480791.1:n.138T>C
XM_005265505.1:c.-26T>C	XP_005265562.1:n.-26T>C
XM_005265506.2:c.-322T>C	XP_005265563.1:n.-322T>C
XM_006713340.2:c.-190T>C	XP_006713403.1:n.-190T>C
XM_006713340.3:c.-190T>C	XP_006713403.1:n.-190T>C
XM_011534147.1:c.140T>C	XP_011532449.1:p.Ile47Thr
XM_011534148.1:c.-190T>C	XP_011532450.1:n.-190T>C
XM_017007302.2:c.-322T>C	XP_016862791.1:n.-322T>C
XM_024453786.1:c.-322T>C	XP_024309554.1:n.-322T>C