Canonical Allele Identifier: CA1941711280

Gene: ACADSB

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123034489A= , CM000672.2:g.123034489A=	GRCh38
NC_000010.10:g.124794005A= , CM000672.1:g.124794005A=	GRCh37
NC_000010.9:g.124783995A=	NCBI36
NG_008003.1:g.30577A= , LRG_451:g.30577A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358776.7:c.176A= MANE Select	ENSP00000357873.3:p.Asp59=
ENST00000358776.6:c.176A=	ENSP00000357873.3:p.Asp59=
ENST00000368869.8:c.-30A=	ENSP00000357862.4:n.-30A=
ENST00000411816.2:n.193A=
NM_001609.3:c.176A= , LRG_451t1:c.176A=	NP_001600.1:p.Asp59=
NM_001330174.1:c.-30A=	NP_001317103.1:n.-30A=
NM_001330174.2:c.-30A=	NP_001317103.1:n.-30A=
NM_001609.4:c.176A= MANE Select	NP_001600.1:p.Asp59=
NM_001330174.3:c.-30A=	NP_001317103.1:n.-30A=