Canonical Allele Identifier: CA2067555805
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1883579092
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739321del , CM000674.2:g.120739321del GRCh38
NC_000012.11:g.121177124del , CM000674.1:g.121177124del GRCh37
NC_000012.10:g.119661507del NCBI36
NG_007991.1:g.18554del

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.1112del MANE Select ENSP00000242592.4:p.Gly371AlafsTer3
ENST00000242592.8:c.1112del ENSP00000242592.4:p.Gly371AlafsTer3
ENST00000411593.2:c.1100del ENSP00000401045.2:p.Gly367AlafsTer3
NM_000017.3:c.1112del NP_000008.1:p.Gly371AlafsTer3
NM_001302554.1:c.1100del NP_001289483.1:p.Gly367AlafsTer3
NM_000017.4:c.1112del MANE Select NP_000008.1:p.Gly371AlafsTer3
NM_001302554.2:c.1100del NP_001289483.1:p.Gly367AlafsTer3
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