Canonical Allele Identifier: CA2611278041
Gene: ACADSB HGNC NCBI

Linked Data

gnomAD v4: 10-123034232-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034237del , CM000672.2:g.123034237del GRCh38
NC_000010.10:g.124793753del , CM000672.1:g.124793753del GRCh37
NC_000010.9:g.124783743del NCBI36
NG_008003.1:g.30325del , LRG_451:g.30325del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.43-119del MANE Select ENSP00000357873.3:n.43-119del
ENST00000358776.6:c.43-119del ENSP00000357873.3:n.43-119del
ENST00000368869.8:c.-163-119del ENSP00000357862.4:n.-163-119del
ENST00000411816.2:n.60-119del
NM_001609.3:c.43-119del , LRG_451t1:c.43-119del NP_001600.1:n.43-119del
NM_001330174.1:c.-163-119del NP_001317103.1:n.-163-119del
NM_001330174.2:c.-163-119del NP_001317103.1:n.-163-119del
NM_001609.4:c.43-119del MANE Select NP_001600.1:n.43-119del
NM_001330174.3:c.-163-119del NP_001317103.1:n.-163-119del
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