Canonical Allele Identifier: CA482146812
Gene: ACADS HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.121176455C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738652C>A , CM000674.2:g.120738652C>A GRCh38
NC_000012.11:g.121176455C>A , CM000674.1:g.121176455C>A GRCh37
NC_000012.10:g.119660838C>A NCBI36
NG_007991.1:g.17885C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.915C>A MANE Select ENSP00000242592.4:p.Thr305=
ENST00000242592.8:c.915C>A ENSP00000242592.4:p.Thr305=
ENST00000411593.2:c.903C>A ENSP00000401045.2:p.Thr301=
NM_000017.3:c.915C>A NP_000008.1:p.Thr305=
NM_001302554.1:c.903C>A NP_001289483.1:p.Thr301=
NM_000017.4:c.915C>A MANE Select NP_000008.1:p.Thr305=
NM_001302554.2:c.903C>A NP_001289483.1:p.Thr301=
Search 100 bp 5'
Search 100 bp 3'