Canonical Allele Identifier: CA1941714572

Gene: ACADSB

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123054042A= , CM000672.2:g.123054042A=	GRCh38
NC_000010.10:g.124813558A= , CM000672.1:g.124813558A=	GRCh37
NC_000010.9:g.124803548A=	NCBI36
NG_008003.1:g.50130A= , LRG_451:g.50130A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000358776.7:c.*277A= MANE Select	ENSP00000357873.3:n.*277A=
ENST00000358776.6:c.*277A=	ENSP00000357873.3:n.*277A=
ENST00000368869.8:c.*277A=	ENSP00000357862.4:n.*277A=
NM_001609.3:c.*277A= , LRG_451t1:c.*277A=	NP_001600.1:n.*277A=
NM_001330174.1:c.*277A=	NP_001317103.1:n.*277A=
NM_001330174.2:c.*277A=	NP_001317103.1:n.*277A=
NM_001609.4:c.*277A= MANE Select	NP_001600.1:n.*277A=
NM_001330174.3:c.*277A=	NP_001317103.1:n.*277A=