Canonical Allele Identifier: CA401067617

Gene: ACOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75955630T>C , CM000679.2:g.75955630T>C	GRCh38
NC_000017.10:g.73951711T>C , CM000679.1:g.73951711T>C	GRCh37
NC_000017.9:g.71463306T>C	NCBI36
NG_008190.1:g.28734A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301608.9:c.710A>G	ENSP00000301608.4:p.Asn237Ser
ENST00000293217.10:c.710A>G MANE Select	ENSP00000293217.4:p.Asn237Ser
ENST00000293217.9:c.710A>G	ENSP00000293217.4:p.Asn237Ser
ENST00000301608.8:c.710A>G	ENSP00000301608.4:p.Asn237Ser
ENST00000572047.5:c.884A>G	ENSP00000459936.1:n.884A>G
ENST00000573078.5:c.*199A>G	ENSP00000458325.1:n.*199A>G
NM_001185039.1:c.596A>G	NP_001171968.1:p.Asn199Ser
NM_004035.6:c.710A>G	NP_004026.2:p.Asn237Ser
NM_007292.5:c.710A>G	NP_009223.2:p.Asn237Ser
XM_011524868.1:c.506A>G	XP_011523170.1:p.Asn169Ser
XM_011524869.1:c.302A>G	XP_011523171.1:p.Asn101Ser
XM_011524868.3:c.506A>G	XP_011523170.1:p.Asn169Ser
XM_011524869.3:c.302A>G	XP_011523171.1:p.Asn101Ser
NM_004035.7:c.710A>G MANE Select	NP_004026.2:p.Asn237Ser
NM_001185039.2:c.596A>G	NP_001171968.1:p.Asn199Ser
NM_007292.6:c.710A>G	NP_009223.2:p.Asn237Ser