Canonical Allele Identifier: CA2067555487
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738763_120738764delinsCT , CM000674.2:g.120738763_120738764delinsCT GRCh38
NC_000012.11:g.121176566_121176567delinsCT , CM000674.1:g.121176566_121176567delinsCT GRCh37
NC_000012.10:g.119660949_119660950delinsCT NCBI36
NG_007991.1:g.17996_17997delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.934-57_934-56delinsCT MANE Select ENSP00000242592.4:n.934-57_934-56delinsCT
ENST00000242592.8:c.934-57_934-56delinsCT ENSP00000242592.4:n.934-57_934-56delinsCT
ENST00000411593.2:c.922-57_922-56delinsCT ENSP00000401045.2:n.922-57_922-56delinsCT
NM_000017.3:c.934-57_934-56delinsCT NP_000008.1:n.934-57_934-56delinsCT
NM_001302554.1:c.922-57_922-56delinsCT NP_001289483.1:n.922-57_922-56delinsCT
NM_000017.4:c.934-57_934-56delinsCT MANE Select NP_000008.1:n.934-57_934-56delinsCT
NM_001302554.2:c.922-57_922-56delinsCT NP_001289483.1:n.922-57_922-56delinsCT