Canonical Allele Identifier: CA1941711358
Gene: ACADSB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034680T= , CM000672.2:g.123034680T= GRCh38
NC_000010.10:g.124794196T= , CM000672.1:g.124794196T= GRCh37
NC_000010.9:g.124784186T= NCBI36
NG_008003.1:g.30768T= , LRG_451:g.30768T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.202+165T= MANE Select ENSP00000357873.3:n.202+165T=
ENST00000358776.6:c.202+165T= ENSP00000357873.3:n.202+165T=
ENST00000368869.8:c.-4+165T= ENSP00000357862.4:n.-4+165T=
ENST00000411816.2:n.219+165T=
NM_001609.3:c.202+165T= , LRG_451t1:c.202+165T= NP_001600.1:n.202+165T=
NM_001330174.1:c.-4+165T= NP_001317103.1:n.-4+165T=
NM_001330174.2:c.-4+165T= NP_001317103.1:n.-4+165T=
NM_001609.4:c.202+165T= MANE Select NP_001600.1:n.202+165T=
NM_001330174.3:c.-4+165T= NP_001317103.1:n.-4+165T=
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