Canonical Allele Identifier: CA358886068
Gene: ACSL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.184764897C>T , CM000666.2:g.184764897C>T GRCh38
NC_000004.11:g.185686051C>T , CM000666.1:g.185686051C>T GRCh37
NC_000004.10:g.185923045C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000503407.6:c.1388G>A ENSP00000425098.2:p.Cys463Tyr
ENST00000505492.2:c.1310G>A ENSP00000425640.2:p.Cys437Tyr
ENST00000706366.1:c.1388G>A ENSP00000516351.1:p.Cys463Tyr
ENST00000706367.1:c.1388G>A ENSP00000516352.1:p.Cys463Tyr
ENST00000706368.1:c.1388G>A ENSP00000516353.1:p.Cys463Tyr
ENST00000706369.1:c.1388G>A ENSP00000516354.1:p.Cys463Tyr
ENST00000706370.1:c.1388G>A ENSP00000516355.1:p.Cys463Tyr
ENST00000281455.7:c.1388G>A MANE Select ENSP00000281455.2:p.Cys463Tyr
ENST00000281455.6:c.1388G>A ENSP00000281455.2:p.Cys463Tyr
ENST00000454703.6:c.875G>A ENSP00000407165.2:p.Cys292Tyr
ENST00000503407.5:c.206G>A ENSP00000425098.1:p.Cys69Tyr
ENST00000504342.5:c.1388G>A ENSP00000425006.1:p.Cys463Tyr
ENST00000506733.5:c.*1142G>A ENSP00000426491.1:n.*1142G>A
ENST00000507295.5:c.1286G>A ENSP00000426244.1:p.Cys429Tyr
ENST00000513317.5:c.1388G>A ENSP00000426150.1:p.Cys463Tyr
ENST00000515030.5:c.1388G>A ENSP00000422607.1:p.Cys463Tyr
ENST00000622937.3:c.875G>A ENSP00000485264.1:p.Cys292Tyr
NM_001286708.1:c.1388G>A NP_001273637.1:p.Cys463Tyr
NM_001286710.1:c.1388G>A NP_001273639.1:p.Cys463Tyr
NM_001286711.1:c.1286G>A NP_001273640.1:p.Cys429Tyr
NM_001286712.1:c.875G>A NP_001273641.1:p.Cys292Tyr
NM_001995.3:c.1388G>A NP_001986.2:p.Cys463Tyr
XM_005262828.1:c.1388G>A XP_005262885.1:p.Cys463Tyr
XM_005262829.1:c.1388G>A XP_005262886.1:p.Cys463Tyr
XM_005262831.1:c.1388G>A XP_005262888.1:p.Cys463Tyr
XM_011531740.1:c.1388G>A XP_011530042.1:p.Cys463Tyr
XM_011531741.1:c.1388G>A XP_011530043.1:p.Cys463Tyr
XM_011531742.1:c.1388G>A XP_011530044.1:p.Cys463Tyr
XM_011531743.1:c.530G>A XP_011530045.1:p.Cys177Tyr
XM_017007887.1:c.1388G>A XP_016863376.1:p.Cys463Tyr
XM_017007888.2:c.1388G>A XP_016863377.1:p.Cys463Tyr
XM_017007889.1:c.1388G>A XP_016863378.1:p.Cys463Tyr
NM_001995.4:c.1388G>A NP_001986.2:p.Cys463Tyr
NM_001286708.2:c.1388G>A NP_001273637.1:p.Cys463Tyr
NM_001286710.2:c.1388G>A NP_001273639.1:p.Cys463Tyr
NM_001286711.2:c.1286G>A NP_001273640.1:p.Cys429Tyr
NM_001381877.1:c.1388G>A NP_001368806.1:p.Cys463Tyr
NM_001381878.1:c.1388G>A NP_001368807.1:p.Cys463Tyr
NM_001381879.1:c.1388G>A NP_001368808.1:p.Cys463Tyr
NM_001381880.1:c.1388G>A NP_001368809.1:p.Cys463Tyr
NM_001381881.1:c.1388G>A NP_001368810.1:p.Cys463Tyr
NM_001381882.1:c.1388G>A NP_001368811.1:p.Cys463Tyr
NM_001381883.1:c.1388G>A NP_001368812.1:p.Cys463Tyr
NM_001381884.1:c.1388G>A NP_001368813.1:p.Cys463Tyr
NM_001381885.1:c.1388G>A NP_001368814.1:p.Cys463Tyr
NM_001381886.1:c.1388G>A NP_001368815.1:p.Cys463Tyr
NM_001381887.1:c.1388G>A NP_001368816.1:p.Cys463Tyr
NM_001381888.1:c.1241G>A NP_001368817.1:p.Cys414Tyr
NM_001381889.1:c.1241G>A NP_001368818.1:p.Cys414Tyr
NM_001381890.1:c.1196G>A NP_001368819.1:p.Cys399Tyr
NM_001995.5:c.1388G>A MANE Select NP_001986.2:p.Cys463Tyr
NR_167698.1:n.1795G>A
NR_167702.1:n.1246G>A
NR_167703.1:n.1246G>A
NR_167704.1:n.1256G>A
NR_167705.1:n.1483G>A
NR_167706.1:n.1519G>A
NR_167708.1:n.1670G>A
NR_167709.1:n.1457G>A