Canonical Allele Identifier: CA1936876618
Gene: ACSL5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.112375157C= , CM000672.2:g.112375157C= GRCh38
NC_000010.10:g.114134915C= , CM000672.1:g.114134915C= GRCh37
NC_000010.9:g.114124905C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000354655.9:c.-30+888C= MANE Select ENSP00000346680.4:n.-30+888C=
ENST00000354655.8:c.-30+888C= ENSP00000346680.4:n.-30+888C=
NM_203379.1:c.-30+888C= NP_976313.1:n.-30+888C=
NM_203379.2:c.-30+888C= MANE Select NP_976313.1:n.-30+888C=
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