Canonical Allele Identifier: CA1519257386

Gene: ACSL1

Genomic Alleles

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

Transcript Alleles

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