Canonical Allele Identifier: CA2067555421
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738639G= , CM000674.2:g.120738639G= GRCh38
NC_000012.11:g.121176442G= , CM000674.1:g.121176442G= GRCh37
NC_000012.10:g.119660825G= NCBI36
NG_007991.1:g.17872G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.902G= MANE Select ENSP00000242592.4:p.Gly301=
ENST00000242592.8:c.902G= ENSP00000242592.4:p.Gly301=
ENST00000411593.2:c.890G= ENSP00000401045.2:p.Gly297=
NM_000017.3:c.902G= NP_000008.1:p.Gly301=
NM_001302554.1:c.890G= NP_001289483.1:p.Gly297=
NM_000017.4:c.902G= MANE Select NP_000008.1:p.Gly301=
NM_001302554.2:c.890G= NP_001289483.1:p.Gly297=