Canonical Allele Identifier: CA1941716772
Gene: ACADSB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123056943A= , CM000672.2:g.123056943A= GRCh38
NC_000010.10:g.124816459A= , CM000672.1:g.124816459A= GRCh37
NC_000010.9:g.124806449A= NCBI36
NG_008003.1:g.53031A= , LRG_451:g.53031A=

Transcript Alleles

HGVS Amino-acid change
ENST00000358776.7:c.*3178A= MANE Select ENSP00000357873.3:n.*3178A=
ENST00000358776.6:c.*3178A= ENSP00000357873.3:n.*3178A=
NM_001609.3:c.*3178A= , LRG_451t1:c.*3178A= NP_001600.1:n.*3178A=
NM_001330174.1:c.*3178A= NP_001317103.1:n.*3178A=
NM_001330174.2:c.*3178A= NP_001317103.1:n.*3178A=
NM_001609.4:c.*3178A= MANE Select NP_001600.1:n.*3178A=
NM_001330174.3:c.*3178A= NP_001317103.1:n.*3178A=