Canonical Allele Identifier: CA1941713628
Gene: ACADSB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123053023T= , CM000672.2:g.123053023T= GRCh38
NC_000010.10:g.124812539T= , CM000672.1:g.124812539T= GRCh37
NC_000010.9:g.124802529T= NCBI36
NG_008003.1:g.49111T= , LRG_451:g.49111T=

Transcript Alleles

HGVS Amino-acid change
ENST00000358776.7:c.1129-38T= MANE Select ENSP00000357873.3:n.1129-38T=
ENST00000358776.6:c.1129-38T= ENSP00000357873.3:n.1129-38T=
ENST00000368869.8:c.823-38T= ENSP00000357862.4:n.823-38T=
ENST00000541070.1:n.263T=
NM_001609.3:c.1129-38T= , LRG_451t1:c.1129-38T= NP_001600.1:n.1129-38T=
NM_001330174.1:c.823-38T= NP_001317103.1:n.823-38T=
NM_001330174.2:c.823-38T= NP_001317103.1:n.823-38T=
NM_001609.4:c.1129-38T= MANE Select NP_001600.1:n.1129-38T=
NM_001330174.3:c.823-38T= NP_001317103.1:n.823-38T=