Canonical Allele Identifier: CA1941711189

Gene: ACADSB

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123034277A= , CM000672.2:g.123034277A=	GRCh38
NC_000010.10:g.124793793A= , CM000672.1:g.124793793A=	GRCh37
NC_000010.9:g.124783783A=	NCBI36
NG_008003.1:g.30365A= , LRG_451:g.30365A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358776.7:c.43-79A= MANE Select	ENSP00000357873.3:n.43-79A=
ENST00000358776.6:c.43-79A=	ENSP00000357873.3:n.43-79A=
ENST00000368869.8:c.-163-79A=	ENSP00000357862.4:n.-163-79A=
ENST00000411816.2:n.60-79A=
NM_001609.3:c.43-79A= , LRG_451t1:c.43-79A=	NP_001600.1:n.43-79A=
NM_001330174.1:c.-163-79A=	NP_001317103.1:n.-163-79A=
NM_001330174.2:c.-163-79A=	NP_001317103.1:n.-163-79A=
NM_001609.4:c.43-79A= MANE Select	NP_001600.1:n.43-79A=
NM_001330174.3:c.-163-79A=	NP_001317103.1:n.-163-79A=