Canonical Allele Identifier: CA2789793028
Gene: ACADSB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034626del , CM000672.2:g.123034626del GRCh38
NC_000010.10:g.124794142del , CM000672.1:g.124794142del GRCh37
NC_000010.9:g.124784132del NCBI36
NG_008003.1:g.30714del , LRG_451:g.30714del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.202+111del MANE Select ENSP00000357873.3:n.202+111del
ENST00000358776.6:c.202+111del ENSP00000357873.3:n.202+111del
ENST00000368869.8:c.-4+111del ENSP00000357862.4:n.-4+111del
ENST00000411816.2:n.219+111del
NM_001609.3:c.202+111del , LRG_451t1:c.202+111del NP_001600.1:n.202+111del
NM_001330174.1:c.-4+111del NP_001317103.1:n.-4+111del
NM_001330174.2:c.-4+111del NP_001317103.1:n.-4+111del
NM_001609.4:c.202+111del MANE Select NP_001600.1:n.202+111del
NM_001330174.3:c.-4+111del NP_001317103.1:n.-4+111del