Canonical Allele Identifier: CA8776649

Gene: ACOX1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75948365A>G , CM000679.2:g.75948365A>G	GRCh38
NC_000017.10:g.73944446A>G , CM000679.1:g.73944446A>G	GRCh37
NC_000017.9:g.71456041A>G	NCBI36
NG_008190.1:g.35999T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004035.7:c.1821T>C MANE Select	NP_004026.2:p.Val607=
ENST00000293217.10:c.1821T>C MANE Select	ENSP00000293217.4:p.Val607=
NM_001185039.1:c.1707T>C	NP_001171968.1:p.Val569=
NM_001185039.2:c.1707T>C	NP_001171968.1:p.Val569=
NM_004035.6:c.1821T>C	NP_004026.2:p.Val607=
NM_007292.5:c.1821T>C	NP_009223.2:p.Val607=
NM_007292.6:c.1821T>C	NP_009223.2:p.Val607=
ENST00000293217.9:c.1821T>C	ENSP00000293217.4:p.Val607=
ENST00000301608.8:c.1821T>C	ENSP00000301608.4:p.Val607=
ENST00000301608.9:c.1821T>C	ENSP00000301608.4:p.Val607=
ENST00000572047.5:c.1995T>C	ENSP00000459936.1:n.1995T>C
ENST00000573078.5:c.*1310T>C	ENSP00000458325.1:n.*1310T>C
ENST00000587927.5:c.236T>C
ENST00000588968.5:c.275T>C
XM_011524868.1:c.1617T>C	XP_011523170.1:p.Val539=
XM_011524868.3:c.1617T>C	XP_011523170.1:p.Val539=
XM_011524869.1:c.1413T>C	XP_011523171.1:p.Val471=
XM_011524869.3:c.1413T>C	XP_011523171.1:p.Val471=