Canonical Allele Identifier: CA482146818
Gene: ACADS HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.121176458G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738655G>A , CM000674.2:g.120738655G>A GRCh38
NC_000012.11:g.121176458G>A , CM000674.1:g.121176458G>A GRCh37
NC_000012.10:g.119660841G>A NCBI36
NG_007991.1:g.17888G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.918G>A MANE Select ENSP00000242592.4:p.Lys306=
ENST00000242592.8:c.918G>A ENSP00000242592.4:p.Lys306=
ENST00000411593.2:c.906G>A ENSP00000401045.2:p.Lys302=
NM_000017.3:c.918G>A NP_000008.1:p.Lys306=
NM_001302554.1:c.906G>A NP_001289483.1:p.Lys302=
NM_000017.4:c.918G>A MANE Select NP_000008.1:p.Lys306=
NM_001302554.2:c.906G>A NP_001289483.1:p.Lys302=