Canonical Allele Identifier: CA2067555417
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738636T= , CM000674.2:g.120738636T= GRCh38
NC_000012.11:g.121176439T= , CM000674.1:g.121176439T= GRCh37
NC_000012.10:g.119660822T= NCBI36
NG_007991.1:g.17869T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.899T= MANE Select ENSP00000242592.4:p.Phe300=
ENST00000242592.8:c.899T= ENSP00000242592.4:p.Phe300=
ENST00000411593.2:c.887T= ENSP00000401045.2:p.Phe296=
NM_000017.3:c.899T= NP_000008.1:p.Phe300=
NM_001302554.1:c.887T= NP_001289483.1:p.Phe296=
NM_000017.4:c.899T= MANE Select NP_000008.1:p.Phe300=
NM_001302554.2:c.887T= NP_001289483.1:p.Phe296=