Canonical Allele Identifier: CA1941711387
Gene: ACADSB HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034729A= , CM000672.2:g.123034729A= GRCh38
NC_000010.10:g.124794245A= , CM000672.1:g.124794245A= GRCh37
NC_000010.9:g.124784235A= NCBI36
NG_008003.1:g.30817A= , LRG_451:g.30817A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.202+214A= MANE Select ENSP00000357873.3:n.202+214A=
ENST00000358776.6:c.202+214A= ENSP00000357873.3:n.202+214A=
ENST00000368869.8:c.-4+214A= ENSP00000357862.4:n.-4+214A=
ENST00000411816.2:n.219+214A=
NM_001609.3:c.202+214A= , LRG_451t1:c.202+214A= NP_001600.1:n.202+214A=
NM_001330174.1:c.-4+214A= NP_001317103.1:n.-4+214A=
NM_001330174.2:c.-4+214A= NP_001317103.1:n.-4+214A=
NM_001609.4:c.202+214A= MANE Select NP_001600.1:n.202+214A=
NM_001330174.3:c.-4+214A= NP_001317103.1:n.-4+214A=
Search 100 bp 5'
Search 100 bp 3'