Canonical Allele Identifier: CA6830799
Gene: ACADS HGNC NCBI

Linked Data

ClinVar Variation Id: 1382300
ClinVar RCV Id: RCV001897570
dbSNP Id: rs774801839

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120737001G>A , CM000674.2:g.120737001G>A GRCh38
NC_000012.11:g.121174804G>A , CM000674.1:g.121174804G>A GRCh37
NC_000012.10:g.119659187G>A NCBI36
NG_007991.1:g.16234G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.226G>A MANE Select ENSP00000242592.4:p.Gly76Arg
ENST00000242592.8:c.226G>A ENSP00000242592.4:p.Gly76Arg
ENST00000411593.2:c.226G>A ENSP00000401045.2:p.Gly76Arg
ENST00000539690.1:n.338G>A
NM_000017.3:c.226G>A NP_000008.1:p.Gly76Arg
NM_001302554.1:c.226G>A NP_001289483.1:p.Gly76Arg
NM_000017.4:c.226G>A MANE Select NP_000008.1:p.Gly76Arg
NM_001302554.2:c.226G>A NP_001289483.1:p.Gly76Arg