Canonical Allele Identifier: CA1941711178

Gene: ACADSB

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123034240C= , CM000672.2:g.123034240C=	GRCh38
NC_000010.10:g.124793756C= , CM000672.1:g.124793756C=	GRCh37
NC_000010.9:g.124783746C=	NCBI36
NG_008003.1:g.30328C= , LRG_451:g.30328C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358776.7:c.43-116C= MANE Select	ENSP00000357873.3:n.43-116C=
ENST00000358776.6:c.43-116C=	ENSP00000357873.3:n.43-116C=
ENST00000368869.8:c.-163-116C=	ENSP00000357862.4:n.-163-116C=
ENST00000411816.2:n.60-116C=
NM_001609.3:c.43-116C= , LRG_451t1:c.43-116C=	NP_001600.1:n.43-116C=
NM_001330174.1:c.-163-116C=	NP_001317103.1:n.-163-116C=
NM_001330174.2:c.-163-116C=	NP_001317103.1:n.-163-116C=
NM_001609.4:c.43-116C= MANE Select	NP_001600.1:n.43-116C=
NM_001330174.3:c.-163-116C=	NP_001317103.1:n.-163-116C=