Canonical Allele Identifier: CA358887053
Gene: ACSL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.184766660T>G , CM000666.2:g.184766660T>G GRCh38
NC_000004.11:g.185687814T>G , CM000666.1:g.185687814T>G GRCh37
NC_000004.10:g.185924808T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000503407.6:c.1225A>C ENSP00000425098.2:p.Asn409His
ENST00000505492.2:c.1147A>C ENSP00000425640.2:p.Asn383His
ENST00000706366.1:c.1225A>C ENSP00000516351.1:p.Asn409His
ENST00000706367.1:c.1225A>C ENSP00000516352.1:p.Asn409His
ENST00000706368.1:c.1225A>C ENSP00000516353.1:p.Asn409His
ENST00000706369.1:c.1225A>C ENSP00000516354.1:p.Asn409His
ENST00000706370.1:c.1225A>C ENSP00000516355.1:p.Asn409His
ENST00000281455.7:c.1225A>C MANE Select ENSP00000281455.2:p.Asn409His
ENST00000281455.6:c.1225A>C ENSP00000281455.2:p.Asn409His
ENST00000454703.6:c.712A>C ENSP00000407165.2:p.Asn238His
ENST00000503407.5:c.43A>C ENSP00000425098.1:p.Asn15His
ENST00000504342.5:c.1225A>C ENSP00000425006.1:p.Asn409His
ENST00000506733.5:c.*979A>C ENSP00000426491.1:n.*979A>C
ENST00000507295.5:c.1123A>C ENSP00000426244.1:p.Asn375His
ENST00000513317.5:c.1225A>C ENSP00000426150.1:p.Asn409His
ENST00000515030.5:c.1225A>C ENSP00000422607.1:p.Asn409His
ENST00000622937.3:c.712A>C ENSP00000485264.1:p.Asn238His
NM_001286708.1:c.1225A>C NP_001273637.1:p.Asn409His
NM_001286710.1:c.1225A>C NP_001273639.1:p.Asn409His
NM_001286711.1:c.1123A>C NP_001273640.1:p.Asn375His
NM_001286712.1:c.712A>C NP_001273641.1:p.Asn238His
NM_001995.3:c.1225A>C NP_001986.2:p.Asn409His
XM_005262828.1:c.1225A>C XP_005262885.1:p.Asn409His
XM_005262829.1:c.1225A>C XP_005262886.1:p.Asn409His
XM_005262831.1:c.1225A>C XP_005262888.1:p.Asn409His
XM_011531740.1:c.1225A>C XP_011530042.1:p.Asn409His
XM_011531741.1:c.1225A>C XP_011530043.1:p.Asn409His
XM_011531742.1:c.1225A>C XP_011530044.1:p.Asn409His
XM_011531743.1:c.367A>C XP_011530045.1:p.Asn123His
XM_017007887.1:c.1225A>C XP_016863376.1:p.Asn409His
XM_017007888.2:c.1225A>C XP_016863377.1:p.Asn409His
XM_017007889.1:c.1225A>C XP_016863378.1:p.Asn409His
NM_001995.4:c.1225A>C NP_001986.2:p.Asn409His
NM_001286708.2:c.1225A>C NP_001273637.1:p.Asn409His
NM_001286710.2:c.1225A>C NP_001273639.1:p.Asn409His
NM_001286711.2:c.1123A>C NP_001273640.1:p.Asn375His
NM_001381877.1:c.1225A>C NP_001368806.1:p.Asn409His
NM_001381878.1:c.1225A>C NP_001368807.1:p.Asn409His
NM_001381879.1:c.1225A>C NP_001368808.1:p.Asn409His
NM_001381880.1:c.1225A>C NP_001368809.1:p.Asn409His
NM_001381881.1:c.1225A>C NP_001368810.1:p.Asn409His
NM_001381882.1:c.1225A>C NP_001368811.1:p.Asn409His
NM_001381883.1:c.1225A>C NP_001368812.1:p.Asn409His
NM_001381884.1:c.1225A>C NP_001368813.1:p.Asn409His
NM_001381885.1:c.1225A>C NP_001368814.1:p.Asn409His
NM_001381886.1:c.1225A>C NP_001368815.1:p.Asn409His
NM_001381887.1:c.1225A>C NP_001368816.1:p.Asn409His
NM_001381888.1:c.1078A>C NP_001368817.1:p.Asn360His
NM_001381889.1:c.1078A>C NP_001368818.1:p.Asn360His
NM_001381890.1:c.1033A>C NP_001368819.1:p.Asn345His
NM_001995.5:c.1225A>C MANE Select NP_001986.2:p.Asn409His
NR_167698.1:n.1632A>C
NR_167702.1:n.1083A>C
NR_167703.1:n.1083A>C
NR_167704.1:n.1093A>C
NR_167705.1:n.1320A>C
NR_167706.1:n.1356A>C
NR_167708.1:n.1507A>C
NR_167709.1:n.1294A>C