Canonical Allele Identifier: CA1941711298
Gene: ACADSB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034530C= , CM000672.2:g.123034530C= GRCh38
NC_000010.10:g.124794046C= , CM000672.1:g.124794046C= GRCh37
NC_000010.9:g.124784036C= NCBI36
NG_008003.1:g.30618C= , LRG_451:g.30618C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.202+15C= MANE Select ENSP00000357873.3:n.202+15C=
ENST00000358776.6:c.202+15C= ENSP00000357873.3:n.202+15C=
ENST00000368869.8:c.-4+15C= ENSP00000357862.4:n.-4+15C=
ENST00000411816.2:n.219+15C=
NM_001609.3:c.202+15C= , LRG_451t1:c.202+15C= NP_001600.1:n.202+15C=
NM_001330174.1:c.-4+15C= NP_001317103.1:n.-4+15C=
NM_001330174.2:c.-4+15C= NP_001317103.1:n.-4+15C=
NM_001609.4:c.202+15C= MANE Select NP_001600.1:n.202+15C=
NM_001330174.3:c.-4+15C= NP_001317103.1:n.-4+15C=
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