Canonical Allele Identifier: CA386601913
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1248673994

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739374G>C , CM000674.2:g.120739374G>C GRCh38
NC_000012.11:g.121177177G>C , CM000674.1:g.121177177G>C GRCh37
NC_000012.10:g.119661560G>C NCBI36
NG_007991.1:g.18607G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.1165G>C MANE Select ENSP00000242592.4:p.Glu389Gln
ENST00000242592.8:c.1165G>C ENSP00000242592.4:p.Glu389Gln
ENST00000411593.2:c.1153G>C ENSP00000401045.2:p.Glu385Gln
NM_000017.3:c.1165G>C NP_000008.1:p.Glu389Gln
NM_001302554.1:c.1153G>C NP_001289483.1:p.Glu385Gln
NM_000017.4:c.1165G>C MANE Select NP_000008.1:p.Glu389Gln
NM_001302554.2:c.1153G>C NP_001289483.1:p.Glu385Gln