Canonical Allele Identifier: CA378618280
Gene: ACADSB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123040608T>C , CM000672.2:g.123040608T>C GRCh38
NC_000010.10:g.124800124T>C , CM000672.1:g.124800124T>C GRCh37
NC_000010.9:g.124790114T>C NCBI36
NG_008003.1:g.36696T>C , LRG_451:g.36696T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000358776.7:c.446T>C MANE Select ENSP00000357873.3:p.Leu149Pro
ENST00000358776.6:c.446T>C ENSP00000357873.3:p.Leu149Pro
ENST00000368869.8:c.140T>C ENSP00000357862.4:p.Leu47Pro
ENST00000411816.2:n.463T>C
NM_001609.3:c.446T>C , LRG_451t1:c.446T>C NP_001600.1:p.Leu149Pro
NM_001330174.1:c.140T>C NP_001317103.1:p.Leu47Pro
NM_001330174.2:c.140T>C NP_001317103.1:p.Leu47Pro
NM_001609.4:c.446T>C MANE Select NP_001600.1:p.Leu149Pro
NM_001330174.3:c.140T>C NP_001317103.1:p.Leu47Pro