Canonical Allele Identifier: CA121574
Gene: ACSL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 11564
ClinVar RCV Id: RCV000012320
dbSNP Id: rs122458138

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.109661643G>T , CM000685.2:g.109661643G>T GRCh38
NC_000023.10:g.108904872G>T , CM000685.1:g.108904872G>T GRCh37
NC_000023.9:g.108791528G>T NCBI36
NG_008053.1:g.76750C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000340800.7:c.1708C>A ENSP00000339787.2:p.Arg570Ser
ENST00000682031.1:c.1552C>A ENSP00000506881.1:p.Arg518Ser
ENST00000683559.1:n.3296C>A
ENST00000684030.1:n.4118C>A
ENST00000684414.1:n.135-17457C>A
ENST00000469796.7:c.1708C>A ENSP00000419171.2:p.Arg570Ser
ENST00000502391.6:c.1708C>A ENSP00000425408.2:p.Arg570Ser
ENST00000671846.1:c.1708C>A ENSP00000500897.1:p.Arg570Ser
ENST00000672282.1:c.1585C>A ENSP00000500678.1:p.Arg529Ser
ENST00000672401.1:c.1585C>A MANE Select ENSP00000500273.1:p.Arg529Ser
ENST00000673016.1:c.1585C>A ENSP00000499969.1:p.Arg529Ser
ENST00000340800.6:c.1708C>A ENSP00000339787.2:p.Arg570Ser
ENST00000348502.10:c.1585C>A ENSP00000262835.7:p.Arg529Ser
ENST00000469796.6:c.1708C>A ENSP00000419171.2:p.Arg570Ser
ENST00000514500.1:c.457+1627C>A
NM_004458.2:c.1585C>A NP_004449.1:p.Arg529Ser
NM_022977.2:c.1708C>A NP_075266.1:p.Arg570Ser
XM_005262108.1:c.1708C>A XP_005262165.1:p.Arg570Ser
XM_005262109.1:c.1708C>A XP_005262166.1:p.Arg570Ser
XM_005262110.1:c.1585C>A XP_005262167.1:p.Arg529Ser
XM_006724635.1:c.1585C>A XP_006724698.1:p.Arg529Ser
XM_011530888.1:c.1708C>A XP_011529190.1:p.Arg570Ser
XM_011530889.1:c.1708C>A XP_011529191.1:p.Arg570Ser
NM_001318509.1:c.1708C>A NP_001305438.1:p.Arg570Ser
NM_001318510.1:c.1585C>A NP_001305439.1:p.Arg529Ser
XM_005262109.2:c.1708C>A XP_005262166.1:p.Arg570Ser
XM_006724635.2:c.1585C>A XP_006724698.1:p.Arg529Ser
XM_011530888.2:c.1708C>A XP_011529190.1:p.Arg570Ser
XM_011530889.2:c.1708C>A XP_011529191.1:p.Arg570Ser
XM_024452351.1:c.1726C>A XP_024308119.1:p.Arg576Ser
NM_001318509.2:c.1708C>A NP_001305438.1:p.Arg570Ser
NM_001318510.2:c.1585C>A MANE Select NP_001305439.1:p.Arg529Ser
NM_004458.3:c.1585C>A NP_004449.1:p.Arg529Ser
NM_022977.3:c.1708C>A NP_075266.1:p.Arg570Ser