Canonical Allele Identifier: CA215157076
Gene: ACADSB HGNC NCBI

Linked Data

dbSNP Id: rs35537376

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034572dup , CM000672.2:g.123034572dup GRCh38
NC_000010.10:g.124794088dup , CM000672.1:g.124794088dup GRCh37
NC_000010.9:g.124784078dup NCBI36
NG_008003.1:g.30660dup , LRG_451:g.30660dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.202+57dup MANE Select ENSP00000357873.3:n.202+57dup
ENST00000358776.6:c.202+57dup ENSP00000357873.3:n.202+57dup
ENST00000368869.8:c.-4+57dup ENSP00000357862.4:n.-4+57dup
ENST00000411816.2:n.219+57dup
NM_001609.3:c.202+57dup , LRG_451t1:c.202+57dup NP_001600.1:n.202+57dup
NM_001330174.1:c.-4+57dup NP_001317103.1:n.-4+57dup
NM_001330174.2:c.-4+57dup NP_001317103.1:n.-4+57dup
NM_001609.4:c.202+57dup MANE Select NP_001600.1:n.202+57dup
NM_001330174.3:c.-4+57dup NP_001317103.1:n.-4+57dup