Canonical Allele Identifier: CA1941711243

Gene: ACADSB

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123034382G= , CM000672.2:g.123034382G=	GRCh38
NC_000010.10:g.124793898G= , CM000672.1:g.124793898G=	GRCh37
NC_000010.9:g.124783888G=	NCBI36
NG_008003.1:g.30470G= , LRG_451:g.30470G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358776.7:c.69G= MANE Select	ENSP00000357873.3:p.Leu23=
ENST00000358776.6:c.69G=	ENSP00000357873.3:p.Leu23=
ENST00000368869.8:c.-137G=	ENSP00000357862.4:n.-137G=
ENST00000411816.2:n.86G=
NM_001609.3:c.69G= , LRG_451t1:c.69G=	NP_001600.1:p.Leu23=
NM_001330174.1:c.-137G=	NP_001317103.1:n.-137G=
NM_001330174.2:c.-137G=	NP_001317103.1:n.-137G=
NM_001609.4:c.69G= MANE Select	NP_001600.1:p.Leu23=
NM_001330174.3:c.-137G=	NP_001317103.1:n.-137G=