Canonical Allele Identifier: CA2067555737
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739185A= , CM000674.2:g.120739185A= GRCh38
NC_000012.11:g.121176988A= , CM000674.1:g.121176988A= GRCh37
NC_000012.10:g.119661371A= NCBI36
NG_007991.1:g.18418A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.1075A= MANE Select ENSP00000242592.4:p.Ile359=
ENST00000242592.8:c.1075A= ENSP00000242592.4:p.Ile359=
ENST00000411593.2:c.1063A= ENSP00000401045.2:p.Ile355=
NM_000017.3:c.1075A= NP_000008.1:p.Ile359=
NM_001302554.1:c.1063A= NP_001289483.1:p.Ile355=
NM_000017.4:c.1075A= MANE Select NP_000008.1:p.Ile359=
NM_001302554.2:c.1063A= NP_001289483.1:p.Ile355=