Canonical Allele Identifier: CA2067555558
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738875_120738876delinsGC , CM000674.2:g.120738875_120738876delinsGC GRCh38
NC_000012.11:g.121176678_121176679delinsGC , CM000674.1:g.121176678_121176679delinsGC GRCh37
NC_000012.10:g.119661061_119661062delinsGC NCBI36
NG_007991.1:g.18108_18109delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.989_990delinsGC MANE Select ENSP00000242592.4:p.Arg330=
ENST00000242592.8:c.989_990delinsGC ENSP00000242592.4:p.Arg330=
ENST00000411593.2:c.977_978delinsGC ENSP00000401045.2:p.Arg326=
NM_000017.3:c.989_990delinsGC NP_000008.1:p.Arg330=
NM_001302554.1:c.977_978delinsGC NP_001289483.1:p.Arg326=
NM_000017.4:c.989_990delinsGC MANE Select NP_000008.1:p.Arg330=
NM_001302554.2:c.977_978delinsGC NP_001289483.1:p.Arg326=