Canonical Allele Identifier: CA414216962

Gene: ACSL4

Linked Data

• dbSNP Id: rs122458139
• gnomAD v3: X-109674403-G-T
• gnomAD v4: X-109674403-G-T
• MyVariant Identifiers: chrX:g.108917632G>T (hg19) ; chrX:g.109674403G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.109674403G>T , CM000685.2:g.109674403G>T	GRCh38
NC_000023.10:g.108917632G>T , CM000685.1:g.108917632G>T	GRCh37
NC_000023.9:g.108804288G>T	NCBI36
NG_008053.1:g.63990C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000340800.7:c.1124C>A	ENSP00000339787.2:p.Pro375Gln
ENST00000682031.1:c.1124C>A	ENSP00000506881.1:p.Pro375Gln
ENST00000683559.1:n.2712C>A
ENST00000684030.1:n.1517C>A
ENST00000684414.1:n.135-30217C>A
ENST00000469796.7:c.1124C>A	ENSP00000419171.2:p.Pro375Gln
ENST00000502391.6:c.1124C>A	ENSP00000425408.2:p.Pro375Gln
ENST00000671846.1:c.1124C>A	ENSP00000500897.1:p.Pro375Gln
ENST00000672282.1:c.1001C>A	ENSP00000500678.1:p.Pro334Gln
ENST00000672401.1:c.1001C>A MANE Select	ENSP00000500273.1:p.Pro334Gln
ENST00000673016.1:c.1001C>A	ENSP00000499969.1:p.Pro334Gln
ENST00000340800.6:c.1124C>A	ENSP00000339787.2:p.Pro375Gln
ENST00000348502.10:c.1001C>A	ENSP00000262835.7:p.Pro334Gln
ENST00000469796.6:c.1124C>A	ENSP00000419171.2:p.Pro375Gln
NM_004458.2:c.1001C>A	NP_004449.1:p.Pro334Gln
NM_022977.2:c.1124C>A	NP_075266.1:p.Pro375Gln
XM_005262108.1:c.1124C>A	XP_005262165.1:p.Pro375Gln
XM_005262109.1:c.1124C>A	XP_005262166.1:p.Pro375Gln
XM_005262110.1:c.1001C>A	XP_005262167.1:p.Pro334Gln
XM_006724635.1:c.1001C>A	XP_006724698.1:p.Pro334Gln
XM_011530888.1:c.1124C>A	XP_011529190.1:p.Pro375Gln
XM_011530889.1:c.1124C>A	XP_011529191.1:p.Pro375Gln
NM_001318509.1:c.1124C>A	NP_001305438.1:p.Pro375Gln
NM_001318510.1:c.1001C>A	NP_001305439.1:p.Pro334Gln
XM_005262109.2:c.1124C>A	XP_005262166.1:p.Pro375Gln
XM_006724635.2:c.1001C>A	XP_006724698.1:p.Pro334Gln
XM_011530888.2:c.1124C>A	XP_011529190.1:p.Pro375Gln
XM_011530889.2:c.1124C>A	XP_011529191.1:p.Pro375Gln
XM_024452351.1:c.1142C>A	XP_024308119.1:p.Pro381Gln
NM_001318509.2:c.1124C>A	NP_001305438.1:p.Pro375Gln
NM_001318510.2:c.1001C>A MANE Select	NP_001305439.1:p.Pro334Gln
NM_004458.3:c.1001C>A	NP_004449.1:p.Pro334Gln
NM_022977.3:c.1124C>A	NP_075266.1:p.Pro375Gln