Canonical Allele Identifier: CA1941716756
Gene: ACADSB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123056920A= , CM000672.2:g.123056920A= GRCh38
NC_000010.10:g.124816436A= , CM000672.1:g.124816436A= GRCh37
NC_000010.9:g.124806426A= NCBI36
NG_008003.1:g.53008A= , LRG_451:g.53008A=

Transcript Alleles

HGVS Amino-acid change
ENST00000358776.7:c.*3155A= MANE Select ENSP00000357873.3:n.*3155A=
ENST00000358776.6:c.*3155A= ENSP00000357873.3:n.*3155A=
NM_001609.3:c.*3155A= , LRG_451t1:c.*3155A= NP_001600.1:n.*3155A=
NM_001330174.1:c.*3155A= NP_001317103.1:n.*3155A=
NM_001330174.2:c.*3155A= NP_001317103.1:n.*3155A=
NM_001609.4:c.*3155A= MANE Select NP_001600.1:n.*3155A=
NM_001330174.3:c.*3155A= NP_001317103.1:n.*3155A=