Canonical Allele Identifier: CA2534796918
Gene: ACADSB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034163C>A , CM000672.2:g.123034163C>A GRCh38
NC_000010.10:g.124793679C>A , CM000672.1:g.124793679C>A GRCh37
NC_000010.9:g.124783669C>A NCBI36
NG_008003.1:g.30251C>A , LRG_451:g.30251C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.43-193C>A MANE Select ENSP00000357873.3:n.43-193C>A
ENST00000358776.6:c.43-193C>A ENSP00000357873.3:n.43-193C>A
ENST00000368869.8:c.-163-193C>A ENSP00000357862.4:n.-163-193C>A
ENST00000411816.2:n.60-193C>A
NM_001609.3:c.43-193C>A , LRG_451t1:c.43-193C>A NP_001600.1:n.43-193C>A
NM_001330174.1:c.-163-193C>A NP_001317103.1:n.-163-193C>A
NM_001330174.2:c.-163-193C>A NP_001317103.1:n.-163-193C>A
NM_001609.4:c.43-193C>A MANE Select NP_001600.1:n.43-193C>A
NM_001330174.3:c.-163-193C>A NP_001317103.1:n.-163-193C>A