Canonical Allele Identifier: CA1941714562

Gene: ACADSB

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123054039T= , CM000672.2:g.123054039T=	GRCh38
NC_000010.10:g.124813555T= , CM000672.1:g.124813555T=	GRCh37
NC_000010.9:g.124803545T=	NCBI36
NG_008003.1:g.50127T= , LRG_451:g.50127T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000358776.7:c.*274T= MANE Select	ENSP00000357873.3:n.*274T=
ENST00000358776.6:c.*274T=	ENSP00000357873.3:n.*274T=
ENST00000368869.8:c.*274T=	ENSP00000357862.4:n.*274T=
NM_001609.3:c.*274T= , LRG_451t1:c.*274T=	NP_001600.1:n.*274T=
NM_001330174.1:c.*274T=	NP_001317103.1:n.*274T=
NM_001330174.2:c.*274T=	NP_001317103.1:n.*274T=
NM_001609.4:c.*274T= MANE Select	NP_001600.1:n.*274T=
NM_001330174.3:c.*274T=	NP_001317103.1:n.*274T=