Canonical Allele Identifier: CA15033890

Gene: ACSL4

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.109719433A>G , CM000685.2:g.109719433A>G	GRCh38
NC_000023.10:g.108962662A>G , CM000685.1:g.108962662A>G	GRCh37
NC_000023.9:g.108849318A>G	NCBI36
NG_008053.1:g.18960T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340800.7:c.-252+13706T>C	ENSP00000339787.2:n.-252+13706T>C
ENST00000682031.1:c.-234+13706T>C	ENSP00000506881.1:n.-234+13706T>C
ENST00000684030.1:n.160+13706T>C
ENST00000684414.1:n.134+13706T>C
ENST00000469796.7:c.-234+13706T>C	ENSP00000419171.2:n.-234+13706T>C
ENST00000502391.6:c.-181+13706T>C	ENSP00000425408.2:n.-181+13706T>C
ENST00000671846.1:c.-120+13706T>C	ENSP00000500897.1:n.-120+13706T>C
ENST00000672282.1:c.-13+13706T>C	ENSP00000500678.1:n.-13+13706T>C
ENST00000672401.1:c.-66+13706T>C MANE Select	ENSP00000500273.1:n.-66+13706T>C
ENST00000673016.1:c.-195+13706T>C	ENSP00000499969.1:n.-195+13706T>C
ENST00000340800.6:c.-252+13706T>C	ENSP00000339787.2:n.-252+13706T>C
ENST00000348502.10:c.-63+13706T>C	ENSP00000262835.7:n.-63+13706T>C
ENST00000469796.6:c.-234+13706T>C	ENSP00000419171.2:n.-234+13706T>C
ENST00000469857.1:c.-252+13706T>C	ENSP00000423077.1:n.-252+13706T>C
ENST00000502391.5:c.-181+13706T>C	ENSP00000425408.1:n.-181+13706T>C
ENST00000504383.1:n.137+13706T>C
ENST00000504980.5:c.-120+13706T>C	ENSP00000421425.1:n.-120+13706T>C
ENST00000508092.5:c.-67+13706T>C	ENSP00000425378.1:n.-67+13706T>C
NM_004458.2:c.-63+13706T>C	NP_004449.1:n.-63+13706T>C
NM_022977.2:c.-252+13706T>C	NP_075266.1:n.-252+13706T>C
XM_005262108.1:c.-234+13706T>C	XP_005262165.1:n.-234+13706T>C
XM_005262109.1:c.-181+13706T>C	XP_005262166.1:n.-181+13706T>C
XM_005262110.1:c.-66+13706T>C	XP_005262167.1:n.-66+13706T>C
XM_006724635.1:c.-13+13706T>C	XP_006724698.1:n.-13+13706T>C
XM_011530888.1:c.-120+13706T>C	XP_011529190.1:n.-120+13706T>C
XM_011530889.1:c.-67+13706T>C	XP_011529191.1:n.-67+13706T>C
NM_001318509.1:c.-234+13706T>C	NP_001305438.1:n.-234+13706T>C
NM_001318510.1:c.-66+13706T>C	NP_001305439.1:n.-66+13706T>C
XM_005262109.2:c.-181+13706T>C	XP_005262166.1:n.-181+13706T>C
XM_006724635.2:c.-13+13706T>C	XP_006724698.1:n.-13+13706T>C
XM_011530888.2:c.-120+13706T>C	XP_011529190.1:n.-120+13706T>C
XM_011530889.2:c.-67+13706T>C	XP_011529191.1:n.-67+13706T>C
XM_024452351.1:c.-54+13706T>C	XP_024308119.1:n.-54+13706T>C
NM_001318509.2:c.-234+13706T>C	NP_001305438.1:n.-234+13706T>C
NM_001318510.2:c.-66+13706T>C MANE Select	NP_001305439.1:n.-66+13706T>C
NM_004458.3:c.-63+13706T>C	NP_004449.1:n.-63+13706T>C
NM_022977.3:c.-252+13706T>C	NP_075266.1:n.-252+13706T>C