Canonical Allele Identifier: CA2067555859
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739406G= , CM000674.2:g.120739406G= GRCh38
NC_000012.11:g.121177209G= , CM000674.1:g.121177209G= GRCh37
NC_000012.10:g.119661592G= NCBI36
NG_007991.1:g.18639G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.1197G= MANE Select ENSP00000242592.4:p.Arg399=
ENST00000242592.8:c.1197G= ENSP00000242592.4:p.Arg399=
ENST00000411593.2:c.1185G= ENSP00000401045.2:p.Arg395=
NM_000017.3:c.1197G= NP_000008.1:p.Arg399=
NM_001302554.1:c.1185G= NP_001289483.1:p.Arg395=
NM_000017.4:c.1197G= MANE Select NP_000008.1:p.Arg399=
NM_001302554.2:c.1185G= NP_001289483.1:p.Arg395=