Canonical Allele Identifier: CA482146788
Gene: ACADS HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.121176668C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738865C>T , CM000674.2:g.120738865C>T GRCh38
NC_000012.11:g.121176668C>T , CM000674.1:g.121176668C>T GRCh37
NC_000012.10:g.119661051C>T NCBI36
NG_007991.1:g.18098C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.979C>T MANE Select ENSP00000242592.4:p.Leu327=
ENST00000242592.8:c.979C>T ENSP00000242592.4:p.Leu327=
ENST00000411593.2:c.967C>T ENSP00000401045.2:p.Leu323=
NM_000017.3:c.979C>T NP_000008.1:p.Leu327=
NM_001302554.1:c.967C>T NP_001289483.1:p.Leu323=
NM_000017.4:c.979C>T MANE Select NP_000008.1:p.Leu327=
NM_001302554.2:c.967C>T NP_001289483.1:p.Leu323=