Canonical Allele Identifier: CA1941711247
Gene: ACADSB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034394G= , CM000672.2:g.123034394G= GRCh38
NC_000010.10:g.124793910G= , CM000672.1:g.124793910G= GRCh37
NC_000010.9:g.124783900G= NCBI36
NG_008003.1:g.30482G= , LRG_451:g.30482G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.81G= MANE Select ENSP00000357873.3:p.Lys27=
ENST00000358776.6:c.81G= ENSP00000357873.3:p.Lys27=
ENST00000368869.8:c.-125G= ENSP00000357862.4:n.-125G=
ENST00000411816.2:n.98G=
NM_001609.3:c.81G= , LRG_451t1:c.81G= NP_001600.1:p.Lys27=
NM_001330174.1:c.-125G= NP_001317103.1:n.-125G=
NM_001330174.2:c.-125G= NP_001317103.1:n.-125G=
NM_001609.4:c.81G= MANE Select NP_001600.1:p.Lys27=
NM_001330174.3:c.-125G= NP_001317103.1:n.-125G=