Canonical Allele Identifier: CA482146698
Gene: ACADS HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.121176628G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738825G>A , CM000674.2:g.120738825G>A GRCh38
NC_000012.11:g.121176628G>A , CM000674.1:g.121176628G>A GRCh37
NC_000012.10:g.119661011G>A NCBI36
NG_007991.1:g.18058G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.939G>A MANE Select ENSP00000242592.4:p.Lys313=
ENST00000242592.8:c.939G>A ENSP00000242592.4:p.Lys313=
ENST00000411593.2:c.927G>A ENSP00000401045.2:p.Lys309=
NM_000017.3:c.939G>A NP_000008.1:p.Lys313=
NM_001302554.1:c.927G>A NP_001289483.1:p.Lys309=
NM_000017.4:c.939G>A MANE Select NP_000008.1:p.Lys313=
NM_001302554.2:c.927G>A NP_001289483.1:p.Lys309=
Search 100 bp 5'
Search 100 bp 3'