Canonical Allele Identifier: CA16214533
Gene: ACSL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.184816689G>A , CM000666.2:g.184816689G>A GRCh38
NC_000004.11:g.185737843G>A , CM000666.1:g.185737843G>A GRCh37
NC_000004.10:g.185974837G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505492.2:c.-33+9227C>T ENSP00000425640.2:n.-33+9227C>T
ENST00000706366.1:c.-33+9227C>T ENSP00000516351.1:n.-33+9227C>T
ENST00000706369.1:c.-33+8477C>T ENSP00000516354.1:n.-33+8477C>T
ENST00000281455.7:c.-33+9227C>T MANE Select ENSP00000281455.2:n.-33+9227C>T
ENST00000281455.6:c.-33+9227C>T ENSP00000281455.2:n.-33+9227C>T
ENST00000454703.6:c.-319+9227C>T ENSP00000407165.2:n.-319+9227C>T
ENST00000504900.5:c.-33+9227C>T ENSP00000424935.1:n.-33+9227C>T
ENST00000507295.5:c.-33+9227C>T ENSP00000426244.1:n.-33+9227C>T
ENST00000515030.5:c.-33+9836C>T ENSP00000422607.1:n.-33+9836C>T
NM_001286711.1:c.-33+9227C>T NP_001273640.1:n.-33+9227C>T
NM_001995.3:c.-33+9227C>T NP_001986.2:n.-33+9227C>T
XM_017007887.1:c.-33+9836C>T XP_016863376.1:n.-33+9836C>T
XM_017007888.2:c.-33+9227C>T XP_016863377.1:n.-33+9227C>T
NM_001995.4:c.-33+9227C>T NP_001986.2:n.-33+9227C>T
NM_001286711.2:c.-33+9227C>T NP_001273640.1:n.-33+9227C>T
NM_001381877.1:c.-97-2712C>T NP_001368806.1:n.-97-2712C>T
NM_001381878.1:c.-33+8477C>T NP_001368807.1:n.-33+8477C>T
NM_001381884.1:c.-33+9227C>T NP_001368813.1:n.-33+9227C>T
NM_001381885.1:c.-97-2712C>T NP_001368814.1:n.-97-2712C>T
NM_001995.5:c.-33+9227C>T MANE Select NP_001986.2:n.-33+9227C>T
NR_167702.1:n.53+9227C>T
NR_167703.1:n.53+9227C>T
NR_167704.1:n.53+9227C>T
NR_167705.1:n.53+9227C>T
NR_167706.1:n.53+9227C>T
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