Canonical Allele Identifier: CA3155496

Gene: ACSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184764856C>T , CM000666.2:g.184764856C>T	GRCh38
NC_000004.11:g.185686010C>T , CM000666.1:g.185686010C>T	GRCh37
NC_000004.10:g.185923004C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503407.6:c.1429G>A	ENSP00000425098.2:p.Ala477Thr
ENST00000505492.2:c.1351G>A	ENSP00000425640.2:p.Ala451Thr
ENST00000706366.1:c.1429G>A	ENSP00000516351.1:p.Ala477Thr
ENST00000706367.1:c.1429G>A	ENSP00000516352.1:p.Ala477Thr
ENST00000706368.1:c.1429G>A	ENSP00000516353.1:p.Ala477Thr
ENST00000706369.1:c.1429G>A	ENSP00000516354.1:p.Ala477Thr
ENST00000706370.1:c.1429G>A	ENSP00000516355.1:p.Ala477Thr
ENST00000281455.7:c.1429G>A MANE Select	ENSP00000281455.2:p.Ala477Thr
ENST00000281455.6:c.1429G>A	ENSP00000281455.2:p.Ala477Thr
ENST00000454703.6:c.916G>A	ENSP00000407165.2:p.Ala306Thr
ENST00000503407.5:c.247G>A	ENSP00000425098.1:p.Ala83Thr
ENST00000504342.5:c.1429G>A	ENSP00000425006.1:p.Ala477Thr
ENST00000506733.5:c.*1183G>A	ENSP00000426491.1:n.*1183G>A
ENST00000507295.5:c.1327G>A	ENSP00000426244.1:p.Ala443Thr
ENST00000513317.5:c.1429G>A	ENSP00000426150.1:p.Ala477Thr
ENST00000515030.5:c.1429G>A	ENSP00000422607.1:p.Ala477Thr
ENST00000622937.3:c.916G>A	ENSP00000485264.1:p.Ala306Thr
NM_001286708.1:c.1429G>A	NP_001273637.1:p.Ala477Thr
NM_001286710.1:c.1429G>A	NP_001273639.1:p.Ala477Thr
NM_001286711.1:c.1327G>A	NP_001273640.1:p.Ala443Thr
NM_001286712.1:c.916G>A	NP_001273641.1:p.Ala306Thr
NM_001995.3:c.1429G>A	NP_001986.2:p.Ala477Thr
XM_005262828.1:c.1429G>A	XP_005262885.1:p.Ala477Thr
XM_005262829.1:c.1429G>A	XP_005262886.1:p.Ala477Thr
XM_005262831.1:c.1429G>A	XP_005262888.1:p.Ala477Thr
XM_011531740.1:c.1429G>A	XP_011530042.1:p.Ala477Thr
XM_011531741.1:c.1429G>A	XP_011530043.1:p.Ala477Thr
XM_011531742.1:c.1429G>A	XP_011530044.1:p.Ala477Thr
XM_011531743.1:c.571G>A	XP_011530045.1:p.Ala191Thr
XM_017007887.1:c.1429G>A	XP_016863376.1:p.Ala477Thr
XM_017007888.2:c.1429G>A	XP_016863377.1:p.Ala477Thr
XM_017007889.1:c.1429G>A	XP_016863378.1:p.Ala477Thr
NM_001995.4:c.1429G>A	NP_001986.2:p.Ala477Thr
NM_001286708.2:c.1429G>A	NP_001273637.1:p.Ala477Thr
NM_001286710.2:c.1429G>A	NP_001273639.1:p.Ala477Thr
NM_001286711.2:c.1327G>A	NP_001273640.1:p.Ala443Thr
NM_001381877.1:c.1429G>A	NP_001368806.1:p.Ala477Thr
NM_001381878.1:c.1429G>A	NP_001368807.1:p.Ala477Thr
NM_001381879.1:c.1429G>A	NP_001368808.1:p.Ala477Thr
NM_001381880.1:c.1429G>A	NP_001368809.1:p.Ala477Thr
NM_001381881.1:c.1429G>A	NP_001368810.1:p.Ala477Thr
NM_001381882.1:c.1429G>A	NP_001368811.1:p.Ala477Thr
NM_001381883.1:c.1429G>A	NP_001368812.1:p.Ala477Thr
NM_001381884.1:c.1429G>A	NP_001368813.1:p.Ala477Thr
NM_001381885.1:c.1429G>A	NP_001368814.1:p.Ala477Thr
NM_001381886.1:c.1429G>A	NP_001368815.1:p.Ala477Thr
NM_001381887.1:c.1429G>A	NP_001368816.1:p.Ala477Thr
NM_001381888.1:c.1282G>A	NP_001368817.1:p.Ala428Thr
NM_001381889.1:c.1282G>A	NP_001368818.1:p.Ala428Thr
NM_001381890.1:c.1237G>A	NP_001368819.1:p.Ala413Thr
NM_001995.5:c.1429G>A MANE Select	NP_001986.2:p.Ala477Thr
NR_167698.1:n.1836G>A
NR_167702.1:n.1287G>A
NR_167703.1:n.1287G>A
NR_167704.1:n.1297G>A
NR_167705.1:n.1524G>A
NR_167706.1:n.1560G>A
NR_167708.1:n.1711G>A
NR_167709.1:n.1498G>A