Canonical Allele Identifier: CA1941711286
Gene: ACADSB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034501T= , CM000672.2:g.123034501T= GRCh38
NC_000010.10:g.124794017T= , CM000672.1:g.124794017T= GRCh37
NC_000010.9:g.124784007T= NCBI36
NG_008003.1:g.30589T= , LRG_451:g.30589T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.188T= MANE Select ENSP00000357873.3:p.Met63=
ENST00000358776.6:c.188T= ENSP00000357873.3:p.Met63=
ENST00000368869.8:c.-18T= ENSP00000357862.4:n.-18T=
ENST00000411816.2:n.205T=
NM_001609.3:c.188T= , LRG_451t1:c.188T= NP_001600.1:p.Met63=
NM_001330174.1:c.-18T= NP_001317103.1:n.-18T=
NM_001330174.2:c.-18T= NP_001317103.1:n.-18T=
NM_001609.4:c.188T= MANE Select NP_001600.1:p.Met63=
NM_001330174.3:c.-18T= NP_001317103.1:n.-18T=