Canonical Allele Identifier: CA1941713638
Gene: ACADSB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123053040A= , CM000672.2:g.123053040A= GRCh38
NC_000010.10:g.124812556A= , CM000672.1:g.124812556A= GRCh37
NC_000010.9:g.124802546A= NCBI36
NG_008003.1:g.49128A= , LRG_451:g.49128A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.1129-21A= MANE Select ENSP00000357873.3:n.1129-21A=
ENST00000358776.6:c.1129-21A= ENSP00000357873.3:n.1129-21A=
ENST00000368869.8:c.823-21A= ENSP00000357862.4:n.823-21A=
ENST00000541070.1:n.280A=
NM_001609.3:c.1129-21A= , LRG_451t1:c.1129-21A= NP_001600.1:n.1129-21A=
NM_001330174.1:c.823-21A= NP_001317103.1:n.823-21A=
NM_001330174.2:c.823-21A= NP_001317103.1:n.823-21A=
NM_001609.4:c.1129-21A= MANE Select NP_001600.1:n.1129-21A=
NM_001330174.3:c.823-21A= NP_001317103.1:n.823-21A=