Canonical Allele Identifier: CA2067555821
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739347C= , CM000674.2:g.120739347C= GRCh38
NC_000012.11:g.121177150C= , CM000674.1:g.121177150C= GRCh37
NC_000012.10:g.119661533C= NCBI36
NG_007991.1:g.18580C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.1138C= MANE Select ENSP00000242592.4:p.Arg380=
ENST00000242592.8:c.1138C= ENSP00000242592.4:p.Arg380=
ENST00000411593.2:c.1126C= ENSP00000401045.2:p.Arg376=
NM_000017.3:c.1138C= NP_000008.1:p.Arg380=
NM_001302554.1:c.1126C= NP_001289483.1:p.Arg376=
NM_000017.4:c.1138C= MANE Select NP_000008.1:p.Arg380=
NM_001302554.2:c.1126C= NP_001289483.1:p.Arg376=