Canonical Allele Identifier: CA386601425
Gene: ACADS HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.121176627A>G (hg19) chr12:g.120738824A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738824A>G , CM000674.2:g.120738824A>G GRCh38
NC_000012.11:g.121176627A>G , CM000674.1:g.121176627A>G GRCh37
NC_000012.10:g.119661010A>G NCBI36
NG_007991.1:g.18057A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.938A>G MANE Select ENSP00000242592.4:p.Lys313Arg
ENST00000242592.8:c.938A>G ENSP00000242592.4:p.Lys313Arg
ENST00000411593.2:c.926A>G ENSP00000401045.2:p.Lys309Arg
NM_000017.3:c.938A>G NP_000008.1:p.Lys313Arg
NM_001302554.1:c.926A>G NP_001289483.1:p.Lys309Arg
NM_000017.4:c.938A>G MANE Select NP_000008.1:p.Lys313Arg
NM_001302554.2:c.926A>G NP_001289483.1:p.Lys309Arg
Search 100 bp 5'
Search 100 bp 3'