Canonical Allele Identifier: CA11711540

Gene: ACSL1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184810288G>A , CM000666.2:g.184810288G>A	GRCh38
NC_000004.11:g.185731442G>A , CM000666.1:g.185731442G>A	GRCh37
NC_000004.10:g.185968436G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505492.2:c.-32-6742C>T	ENSP00000425640.2:n.-32-6742C>T
ENST00000706366.1:c.-32-6742C>T	ENSP00000516351.1:n.-32-6742C>T
ENST00000706367.1:c.-33+3625C>T	ENSP00000516352.1:n.-33+3625C>T
ENST00000706369.1:c.-32-6742C>T	ENSP00000516354.1:n.-32-6742C>T
ENST00000281455.7:c.-32-6742C>T MANE Select	ENSP00000281455.2:n.-32-6742C>T
ENST00000281455.6:c.-32-6742C>T	ENSP00000281455.2:n.-32-6742C>T
ENST00000454703.6:c.-319+15628C>T	ENSP00000407165.2:n.-319+15628C>T
ENST00000504342.5:c.-33+1872C>T	ENSP00000425006.1:n.-33+1872C>T
ENST00000504900.5:c.-32-6742C>T	ENSP00000424935.1:n.-32-6742C>T
ENST00000507295.5:c.-32-6742C>T	ENSP00000426244.1:n.-32-6742C>T
ENST00000515030.5:c.-32-6742C>T	ENSP00000422607.1:n.-32-6742C>T
NM_001286708.1:c.-33+1872C>T	NP_001273637.1:n.-33+1872C>T
NM_001286711.1:c.-32-6742C>T	NP_001273640.1:n.-32-6742C>T
NM_001995.3:c.-32-6742C>T	NP_001986.2:n.-32-6742C>T
XM_011531740.1:c.-33+1891C>T	XP_011530042.1:n.-33+1891C>T
XM_011531741.1:c.-33+1891C>T	XP_011530043.1:n.-33+1891C>T
XM_011531742.1:c.-33+4710C>T	XP_011530044.1:n.-33+4710C>T
XM_017007887.1:c.-32-6742C>T	XP_016863376.1:n.-32-6742C>T
XM_017007888.2:c.-32-6742C>T	XP_016863377.1:n.-32-6742C>T
NM_001995.4:c.-32-6742C>T	NP_001986.2:n.-32-6742C>T
NM_001286708.2:c.-33+1872C>T	NP_001273637.1:n.-33+1872C>T
NM_001286711.2:c.-32-6742C>T	NP_001273640.1:n.-32-6742C>T
NM_001381877.1:c.-33+3625C>T	NP_001368806.1:n.-33+3625C>T
NM_001381878.1:c.-32-6742C>T	NP_001368807.1:n.-32-6742C>T
NM_001381879.1:c.-33+3625C>T	NP_001368808.1:n.-33+3625C>T
NM_001381880.1:c.-33+4710C>T	NP_001368809.1:n.-33+4710C>T
NM_001381884.1:c.-32-6742C>T	NP_001368813.1:n.-32-6742C>T
NM_001381885.1:c.-33+3625C>T	NP_001368814.1:n.-33+3625C>T
NM_001995.5:c.-32-6742C>T MANE Select	NP_001986.2:n.-32-6742C>T
NR_167702.1:n.53+15628C>T
NR_167703.1:n.53+15628C>T
NR_167704.1:n.53+15628C>T
NR_167705.1:n.54-6742C>T
NR_167706.1:n.54-6742C>T