Canonical Allele Identifier: CA1941711240

Gene: ACADSB

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123034379T= , CM000672.2:g.123034379T=	GRCh38
NC_000010.10:g.124793895T= , CM000672.1:g.124793895T=	GRCh37
NC_000010.9:g.124783885T=	NCBI36
NG_008003.1:g.30467T= , LRG_451:g.30467T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358776.7:c.66T= MANE Select	ENSP00000357873.3:p.Cys22=
ENST00000358776.6:c.66T=	ENSP00000357873.3:p.Cys22=
ENST00000368869.8:c.-140T=	ENSP00000357862.4:n.-140T=
ENST00000411816.2:n.83T=
NM_001609.3:c.66T= , LRG_451t1:c.66T=	NP_001600.1:p.Cys22=
NM_001330174.1:c.-140T=	NP_001317103.1:n.-140T=
NM_001330174.2:c.-140T=	NP_001317103.1:n.-140T=
NM_001609.4:c.66T= MANE Select	NP_001600.1:p.Cys22=
NM_001330174.3:c.-140T=	NP_001317103.1:n.-140T=