Canonical Allele Identifier: CA145599
Gene: ACADS HGNC NCBI

Linked Data

ClinVar Variation Id: 3831
dbSNP Id: rs1799958

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738280G>A , CM000674.2:g.120738280G>A GRCh38
NC_000012.11:g.121176083G>A , CM000674.1:g.121176083G>A GRCh37
NC_000012.10:g.119660466G>A NCBI36
NG_007991.1:g.17513G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.625G>A MANE Select ENSP00000242592.4:p.Gly209Ser
ENST00000242592.8:c.625G>A ENSP00000242592.4:p.Gly209Ser
ENST00000411593.2:c.613G>A ENSP00000401045.2:p.Gly205Ser
NM_000017.3:c.625G>A NP_000008.1:p.Gly209Ser
NM_001302554.1:c.613G>A NP_001289483.1:p.Gly205Ser
NM_000017.4:c.625G>A MANE Select NP_000008.1:p.Gly209Ser
NM_001302554.2:c.613G>A NP_001289483.1:p.Gly205Ser