Canonical Allele Identifier: CA2067555428
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738652C= , CM000674.2:g.120738652C= GRCh38
NC_000012.11:g.121176455C= , CM000674.1:g.121176455C= GRCh37
NC_000012.10:g.119660838C= NCBI36
NG_007991.1:g.17885C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.915C= MANE Select ENSP00000242592.4:p.Thr305=
ENST00000242592.8:c.915C= ENSP00000242592.4:p.Thr305=
ENST00000411593.2:c.903C= ENSP00000401045.2:p.Thr301=
NM_000017.3:c.915C= NP_000008.1:p.Thr305=
NM_001302554.1:c.903C= NP_001289483.1:p.Thr301=
NM_000017.4:c.915C= MANE Select NP_000008.1:p.Thr305=
NM_001302554.2:c.903C= NP_001289483.1:p.Thr301=