Canonical Allele Identifier: CA378615784
Gene: ACADSB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034414A>T , CM000672.2:g.123034414A>T GRCh38
NC_000010.10:g.124793930A>T , CM000672.1:g.124793930A>T GRCh37
NC_000010.9:g.124783920A>T NCBI36
NG_008003.1:g.30502A>T , LRG_451:g.30502A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.101A>T MANE Select ENSP00000357873.3:p.Lys34Ile
ENST00000358776.6:c.101A>T ENSP00000357873.3:p.Lys34Ile
ENST00000368869.8:c.-105A>T ENSP00000357862.4:n.-105A>T
ENST00000411816.2:n.118A>T
NM_001609.3:c.101A>T , LRG_451t1:c.101A>T NP_001600.1:p.Lys34Ile
NM_001330174.1:c.-105A>T NP_001317103.1:n.-105A>T
NM_001330174.2:c.-105A>T NP_001317103.1:n.-105A>T
NM_001609.4:c.101A>T MANE Select NP_001600.1:p.Lys34Ile
NM_001330174.3:c.-105A>T NP_001317103.1:n.-105A>T