Canonical Allele Identifier: CA1941713619
Gene: ACADSB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123053012T= , CM000672.2:g.123053012T= GRCh38
NC_000010.10:g.124812528T= , CM000672.1:g.124812528T= GRCh37
NC_000010.9:g.124802518T= NCBI36
NG_008003.1:g.49100T= , LRG_451:g.49100T=

Transcript Alleles

HGVS Amino-acid change
ENST00000358776.7:c.1129-49T= MANE Select ENSP00000357873.3:n.1129-49T=
ENST00000358776.6:c.1129-49T= ENSP00000357873.3:n.1129-49T=
ENST00000368869.8:c.823-49T= ENSP00000357862.4:n.823-49T=
ENST00000541070.1:n.252T=
NM_001609.3:c.1129-49T= , LRG_451t1:c.1129-49T= NP_001600.1:n.1129-49T=
NM_001330174.1:c.823-49T= NP_001317103.1:n.823-49T=
NM_001330174.2:c.823-49T= NP_001317103.1:n.823-49T=
NM_001609.4:c.1129-49T= MANE Select NP_001600.1:n.1129-49T=
NM_001330174.3:c.823-49T= NP_001317103.1:n.823-49T=