Canonical Allele Identifier: CA2611278050
Gene: ACADSB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034249_123034250del , CM000672.2:g.123034249_123034250del GRCh38
NC_000010.10:g.124793765_124793766del , CM000672.1:g.124793765_124793766del GRCh37
NC_000010.9:g.124783755_124783756del NCBI36
NG_008003.1:g.30337_30338del , LRG_451:g.30337_30338del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.43-107_43-106del MANE Select ENSP00000357873.3:n.43-107_43-106del
ENST00000358776.6:c.43-107_43-106del ENSP00000357873.3:n.43-107_43-106del
ENST00000368869.8:c.-163-107_-163-106del ENSP00000357862.4:n.-163-107_-163-106del
ENST00000411816.2:n.60-107_60-106del
NM_001609.3:c.43-107_43-106del , LRG_451t1:c.43-107_43-106del NP_001600.1:n.43-107_43-106del
NM_001330174.1:c.-163-107_-163-106del NP_001317103.1:n.-163-107_-163-106del
NM_001330174.2:c.-163-107_-163-106del NP_001317103.1:n.-163-107_-163-106del
NM_001609.4:c.43-107_43-106del MANE Select NP_001600.1:n.43-107_43-106del
NM_001330174.3:c.-163-107_-163-106del NP_001317103.1:n.-163-107_-163-106del