Canonical Allele Identifier: CA401065257

Gene: ACOX1

Linked Data

• MyVariant Identifiers: chr17:g.73949562G>T (hg19) ; chr17:g.75953481G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75953481G>T , CM000679.2:g.75953481G>T	GRCh38
NC_000017.10:g.73949562G>T , CM000679.1:g.73949562G>T	GRCh37
NC_000017.9:g.71461157G>T	NCBI36
NG_008190.1:g.30883C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301608.9:c.914C>A	ENSP00000301608.4:p.Ala305Asp
ENST00000293217.10:c.914C>A MANE Select	ENSP00000293217.4:p.Ala305Asp
ENST00000293217.9:c.914C>A	ENSP00000293217.4:p.Ala305Asp
ENST00000301608.8:c.914C>A	ENSP00000301608.4:p.Ala305Asp
ENST00000572047.5:c.1088C>A	ENSP00000459936.1:n.1088C>A
ENST00000573078.5:c.*403C>A	ENSP00000458325.1:n.*403C>A
ENST00000589744.1:n.164C>A
NM_001185039.1:c.800C>A	NP_001171968.1:p.Ala267Asp
NM_004035.6:c.914C>A	NP_004026.2:p.Ala305Asp
NM_007292.5:c.914C>A	NP_009223.2:p.Ala305Asp
XM_011524868.1:c.710C>A	XP_011523170.1:p.Ala237Asp
XM_011524869.1:c.506C>A	XP_011523171.1:p.Ala169Asp
XM_011524868.3:c.710C>A	XP_011523170.1:p.Ala237Asp
XM_011524869.3:c.506C>A	XP_011523171.1:p.Ala169Asp
NM_004035.7:c.914C>A MANE Select	NP_004026.2:p.Ala305Asp
NM_001185039.2:c.800C>A	NP_001171968.1:p.Ala267Asp
NM_007292.6:c.914C>A	NP_009223.2:p.Ala305Asp