Canonical Allele Identifier: CA2067555839
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739374G= , CM000674.2:g.120739374G= GRCh38
NC_000012.11:g.121177177G= , CM000674.1:g.121177177G= GRCh37
NC_000012.10:g.119661560G= NCBI36
NG_007991.1:g.18607G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.1165G= MANE Select ENSP00000242592.4:p.Glu389=
ENST00000242592.8:c.1165G= ENSP00000242592.4:p.Glu389=
ENST00000411593.2:c.1153G= ENSP00000401045.2:p.Glu385=
NM_000017.3:c.1165G= NP_000008.1:p.Glu389=
NM_001302554.1:c.1153G= NP_001289483.1:p.Glu385=
NM_000017.4:c.1165G= MANE Select NP_000008.1:p.Glu389=
NM_001302554.2:c.1153G= NP_001289483.1:p.Glu385=