Canonical Allele Identifier: CA386601980
Gene: ACADS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739402A>G , CM000674.2:g.120739402A>G GRCh38
NC_000012.11:g.121177205A>G , CM000674.1:g.121177205A>G GRCh37
NC_000012.10:g.119661588A>G NCBI36
NG_007991.1:g.18635A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.1193A>G MANE Select ENSP00000242592.4:p.Gln398Arg
ENST00000242592.8:c.1193A>G ENSP00000242592.4:p.Gln398Arg
ENST00000411593.2:c.1181A>G ENSP00000401045.2:p.Gln394Arg
NM_000017.3:c.1193A>G NP_000008.1:p.Gln398Arg
NM_001302554.1:c.1181A>G NP_001289483.1:p.Gln394Arg
NM_000017.4:c.1193A>G MANE Select NP_000008.1:p.Gln398Arg
NM_001302554.2:c.1181A>G NP_001289483.1:p.Gln394Arg