Canonical Allele Identifier: CA2611279692
Gene: ACADSB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123052994A>T , CM000672.2:g.123052994A>T GRCh38
NC_000010.10:g.124812510A>T , CM000672.1:g.124812510A>T GRCh37
NC_000010.9:g.124802500A>T NCBI36
NG_008003.1:g.49082A>T , LRG_451:g.49082A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000358776.7:c.1129-67A>T MANE Select ENSP00000357873.3:n.1129-67A>T
ENST00000358776.6:c.1129-67A>T ENSP00000357873.3:n.1129-67A>T
ENST00000368869.8:c.823-67A>T ENSP00000357862.4:n.823-67A>T
ENST00000541070.1:n.234A>T
NM_001609.3:c.1129-67A>T , LRG_451t1:c.1129-67A>T NP_001600.1:n.1129-67A>T
NM_001330174.1:c.823-67A>T NP_001317103.1:n.823-67A>T
NM_001330174.2:c.823-67A>T NP_001317103.1:n.823-67A>T
NM_001609.4:c.1129-67A>T MANE Select NP_001600.1:n.1129-67A>T
NM_001330174.3:c.823-67A>T NP_001317103.1:n.823-67A>T