Canonical Allele Identifier: CA2067555489
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738763C= , CM000674.2:g.120738763C= GRCh38
NC_000012.11:g.121176566C= , CM000674.1:g.121176566C= GRCh37
NC_000012.10:g.119660949C= NCBI36
NG_007991.1:g.17996C=

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.934-57C= MANE Select ENSP00000242592.4:n.934-57C=
ENST00000242592.8:c.934-57C= ENSP00000242592.4:n.934-57C=
ENST00000411593.2:c.922-57C= ENSP00000401045.2:n.922-57C=
NM_000017.3:c.934-57C= NP_000008.1:n.934-57C=
NM_001302554.1:c.922-57C= NP_001289483.1:n.922-57C=
NM_000017.4:c.934-57C= MANE Select NP_000008.1:n.934-57C=
NM_001302554.2:c.922-57C= NP_001289483.1:n.922-57C=