Canonical Allele Identifier: CA2611278125
Gene: ACADSB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034610_123034614del , CM000672.2:g.123034610_123034614del GRCh38
NC_000010.10:g.124794126_124794130del , CM000672.1:g.124794126_124794130del GRCh37
NC_000010.9:g.124784116_124784120del NCBI36
NG_008003.1:g.30698_30702del , LRG_451:g.30698_30702del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.202+95_202+99del MANE Select ENSP00000357873.3:n.202+95_202+99del
ENST00000358776.6:c.202+95_202+99del ENSP00000357873.3:n.202+95_202+99del
ENST00000368869.8:c.-4+95_-4+99del ENSP00000357862.4:n.-4+95_-4+99del
ENST00000411816.2:n.219+95_219+99del
NM_001609.3:c.202+95_202+99del , LRG_451t1:c.202+95_202+99del NP_001600.1:n.202+95_202+99del
NM_001330174.1:c.-4+95_-4+99del NP_001317103.1:n.-4+95_-4+99del
NM_001330174.2:c.-4+95_-4+99del NP_001317103.1:n.-4+95_-4+99del
NM_001609.4:c.202+95_202+99del MANE Select NP_001600.1:n.202+95_202+99del
NM_001330174.3:c.-4+95_-4+99del NP_001317103.1:n.-4+95_-4+99del