Canonical Allele Identifier: CA6830833
Gene: ACADS HGNC NCBI

Linked Data

ClinVar Variation Id: 2180419
ClinVar RCV Id: RCV002619244
dbSNP Id: rs773156731

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120737134A>G , CM000674.2:g.120737134A>G GRCh38
NC_000012.11:g.121174937A>G , CM000674.1:g.121174937A>G GRCh37
NC_000012.10:g.119659320A>G NCBI36
NG_007991.1:g.16367A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.359A>G MANE Select ENSP00000242592.4:p.Asn120Ser
ENST00000242592.8:c.359A>G ENSP00000242592.4:p.Asn120Ser
ENST00000411593.2:c.359A>G ENSP00000401045.2:p.Asn120Ser
ENST00000539690.1:n.471A>G
NM_000017.3:c.359A>G NP_000008.1:p.Asn120Ser
NM_001302554.1:c.359A>G NP_001289483.1:p.Asn120Ser
NM_000017.4:c.359A>G MANE Select NP_000008.1:p.Asn120Ser
NM_001302554.2:c.359A>G NP_001289483.1:p.Asn120Ser