Canonical Allele Identifier: CA2606931802

Gene: ACSL1

Linked Data

• dbSNP Id: rs1764157423
• gnomAD v3: 4-184769434-C-G
• gnomAD v4: 4-184769434-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184769434C>G , CM000666.2:g.184769434C>G	GRCh38
NC_000004.11:g.185690588C>G , CM000666.1:g.185690588C>G	GRCh37
NC_000004.10:g.185927582C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503407.6:c.993+965G>C	ENSP00000425098.2:n.993+965G>C
ENST00000505492.2:c.916-984G>C	ENSP00000425640.2:n.916-984G>C
ENST00000706366.1:c.993+821G>C	ENSP00000516351.1:n.993+821G>C
ENST00000706367.1:c.993+965G>C	ENSP00000516352.1:n.993+965G>C
ENST00000706368.1:c.993+821G>C	ENSP00000516353.1:n.993+821G>C
ENST00000706369.1:c.993+965G>C	ENSP00000516354.1:n.993+965G>C
ENST00000706370.1:c.993+965G>C	ENSP00000516355.1:n.993+965G>C
ENST00000281455.7:c.993+965G>C MANE Select	ENSP00000281455.2:n.993+965G>C
ENST00000281455.6:c.993+965G>C	ENSP00000281455.2:n.993+965G>C
ENST00000454703.6:c.480+965G>C	ENSP00000407165.2:n.480+965G>C
ENST00000504342.5:c.993+965G>C	ENSP00000425006.1:n.993+965G>C
ENST00000504900.5:c.993+965G>C	ENSP00000424935.1:n.993+965G>C
ENST00000505492.1:c.158-984G>C
ENST00000506733.5:c.*747+965G>C	ENSP00000426491.1:n.*747+965G>C
ENST00000507295.5:c.891+965G>C	ENSP00000426244.1:n.891+965G>C
ENST00000513317.5:c.993+821G>C	ENSP00000426150.1:n.993+821G>C
ENST00000515030.5:c.993+965G>C	ENSP00000422607.1:n.993+965G>C
ENST00000622937.3:c.480+965G>C	ENSP00000485264.1:n.480+965G>C
NM_001286708.1:c.993+965G>C	NP_001273637.1:n.993+965G>C
NM_001286710.1:c.993+821G>C	NP_001273639.1:n.993+821G>C
NM_001286711.1:c.891+965G>C	NP_001273640.1:n.891+965G>C
NM_001286712.1:c.480+965G>C	NP_001273641.1:n.480+965G>C
NM_001995.3:c.993+965G>C	NP_001986.2:n.993+965G>C
XM_005262828.1:c.993+965G>C	XP_005262885.1:n.993+965G>C
XM_005262829.1:c.993+965G>C	XP_005262886.1:n.993+965G>C
XM_005262831.1:c.993+965G>C	XP_005262888.1:n.993+965G>C
XM_011531740.1:c.993+965G>C	XP_011530042.1:n.993+965G>C
XM_011531741.1:c.993+821G>C	XP_011530043.1:n.993+821G>C
XM_011531742.1:c.993+965G>C	XP_011530044.1:n.993+965G>C
XM_011531743.1:c.135+965G>C	XP_011530045.1:n.135+965G>C
XM_017007887.1:c.993+965G>C	XP_016863376.1:n.993+965G>C
XM_017007888.2:c.993+821G>C	XP_016863377.1:n.993+821G>C
XM_017007889.1:c.993+821G>C	XP_016863378.1:n.993+821G>C
NM_001995.4:c.993+965G>C	NP_001986.2:n.993+965G>C
NM_001286708.2:c.993+965G>C	NP_001273637.1:n.993+965G>C
NM_001286710.2:c.993+821G>C	NP_001273639.1:n.993+821G>C
NM_001286711.2:c.891+965G>C	NP_001273640.1:n.891+965G>C
NM_001381877.1:c.993+965G>C	NP_001368806.1:n.993+965G>C
NM_001381878.1:c.993+965G>C	NP_001368807.1:n.993+965G>C
NM_001381879.1:c.993+965G>C	NP_001368808.1:n.993+965G>C
NM_001381880.1:c.993+965G>C	NP_001368809.1:n.993+965G>C
NM_001381881.1:c.993+965G>C	NP_001368810.1:n.993+965G>C
NM_001381882.1:c.993+965G>C	NP_001368811.1:n.993+965G>C
NM_001381883.1:c.993+965G>C	NP_001368812.1:n.993+965G>C
NM_001381884.1:c.993+821G>C	NP_001368813.1:n.993+821G>C
NM_001381885.1:c.993+821G>C	NP_001368814.1:n.993+821G>C
NM_001381886.1:c.993+821G>C	NP_001368815.1:n.993+821G>C
NM_001381887.1:c.993+821G>C	NP_001368816.1:n.993+821G>C
NM_001381888.1:c.846+965G>C	NP_001368817.1:n.846+965G>C
NM_001381889.1:c.846+965G>C	NP_001368818.1:n.846+965G>C
NM_001381890.1:c.801+965G>C	NP_001368819.1:n.801+965G>C
NM_001995.5:c.993+965G>C MANE Select	NP_001986.2:n.993+965G>C
NR_167698.1:n.1400+965G>C
NR_167702.1:n.851+821G>C
NR_167703.1:n.851+965G>C
NR_167704.1:n.861+965G>C
NR_167705.1:n.1088+965G>C
NR_167706.1:n.1124+965G>C
NR_167708.1:n.1275+965G>C
NR_167709.1:n.1062+965G>C