Canonical Allele Identifier: CA1941711234

Gene: ACADSB

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123034370C= , CM000672.2:g.123034370C=	GRCh38
NC_000010.10:g.124793886C= , CM000672.1:g.124793886C=	GRCh37
NC_000010.9:g.124783876C=	NCBI36
NG_008003.1:g.30458C= , LRG_451:g.30458C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358776.7:c.57C= MANE Select	ENSP00000357873.3:p.Phe19=
ENST00000358776.6:c.57C=	ENSP00000357873.3:p.Phe19=
ENST00000368869.8:c.-149C=	ENSP00000357862.4:n.-149C=
ENST00000411816.2:n.74C=
NM_001609.3:c.57C= , LRG_451t1:c.57C=	NP_001600.1:p.Phe19=
NM_001330174.1:c.-149C=	NP_001317103.1:n.-149C=
NM_001330174.2:c.-149C=	NP_001317103.1:n.-149C=
NM_001609.4:c.57C= MANE Select	NP_001600.1:p.Phe19=
NM_001330174.3:c.-149C=	NP_001317103.1:n.-149C=