Canonical Allele Identifier: CA2611279649
Gene: ACADSB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123052951_123052952del , CM000672.2:g.123052951_123052952del GRCh38
NC_000010.10:g.124812467_124812468del , CM000672.1:g.124812467_124812468del GRCh37
NC_000010.9:g.124802457_124802458del NCBI36
NG_008003.1:g.49039_49040del , LRG_451:g.49039_49040del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.1129-110_1129-109del MANE Select ENSP00000357873.3:n.1129-110_1129-109del
ENST00000358776.6:c.1129-110_1129-109del ENSP00000357873.3:n.1129-110_1129-109del
ENST00000368869.8:c.823-110_823-109del ENSP00000357862.4:n.823-110_823-109del
ENST00000541070.1:n.191_192del
NM_001609.3:c.1129-110_1129-109del , LRG_451t1:c.1129-110_1129-109del NP_001600.1:n.1129-110_1129-109del
NM_001330174.1:c.823-110_823-109del NP_001317103.1:n.823-110_823-109del
NM_001330174.2:c.823-110_823-109del NP_001317103.1:n.823-110_823-109del
NM_001609.4:c.1129-110_1129-109del MANE Select NP_001600.1:n.1129-110_1129-109del
NM_001330174.3:c.823-110_823-109del NP_001317103.1:n.823-110_823-109del