Canonical Allele Identifier: CA2067555559
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738876C= , CM000674.2:g.120738876C= GRCh38
NC_000012.11:g.121176679C= , CM000674.1:g.121176679C= GRCh37
NC_000012.10:g.119661062C= NCBI36
NG_007991.1:g.18109C=

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.990C= MANE Select ENSP00000242592.4:p.Arg330=
ENST00000242592.8:c.990C= ENSP00000242592.4:p.Arg330=
ENST00000411593.2:c.978C= ENSP00000401045.2:p.Arg326=
NM_000017.3:c.990C= NP_000008.1:p.Arg330=
NM_001302554.1:c.978C= NP_001289483.1:p.Arg326=
NM_000017.4:c.990C= MANE Select NP_000008.1:p.Arg330=
NM_001302554.2:c.978C= NP_001289483.1:p.Arg326=