Canonical Allele Identifier: CA6831200
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs759011410

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739181C>A , CM000674.2:g.120739181C>A GRCh38
NC_000012.11:g.121176984C>A , CM000674.1:g.121176984C>A GRCh37
NC_000012.10:g.119661367C>A NCBI36
NG_007991.1:g.18414C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.1071C>A MANE Select ENSP00000242592.4:p.Thr357=
ENST00000242592.8:c.1071C>A ENSP00000242592.4:p.Thr357=
ENST00000411593.2:c.1059C>A ENSP00000401045.2:p.Thr353=
NM_000017.3:c.1071C>A NP_000008.1:p.Thr357=
NM_001302554.1:c.1059C>A NP_001289483.1:p.Thr353=
NM_000017.4:c.1071C>A MANE Select NP_000008.1:p.Thr357=
NM_001302554.2:c.1059C>A NP_001289483.1:p.Thr353=