Canonical Allele Identifier: CA2067555432
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738666T= , CM000674.2:g.120738666T= GRCh38
NC_000012.11:g.121176469T= , CM000674.1:g.121176469T= GRCh37
NC_000012.10:g.119660852T= NCBI36
NG_007991.1:g.17899T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.929T= MANE Select ENSP00000242592.4:p.Ile310=
ENST00000242592.8:c.929T= ENSP00000242592.4:p.Ile310=
ENST00000411593.2:c.917T= ENSP00000401045.2:p.Ile306=
NM_000017.3:c.929T= NP_000008.1:p.Ile310=
NM_001302554.1:c.917T= NP_001289483.1:p.Ile306=
NM_000017.4:c.929T= MANE Select NP_000008.1:p.Ile310=
NM_001302554.2:c.917T= NP_001289483.1:p.Ile306=