Canonical Allele Identifier: CA1941714447

Gene: ACADSB

Linked Data

• dbSNP Id: rs1850669206
• gnomAD v4: 10-123053918-T-TTTTGGTTTTCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123053922_123053933dup , CM000672.2:g.123053922_123053933dup	GRCh38
NC_000010.10:g.124813438_124813449dup , CM000672.1:g.124813438_124813449dup	GRCh37
NC_000010.9:g.124803428_124803439dup	NCBI36
NG_008003.1:g.50010_50021dup , LRG_451:g.50010_50021dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000358776.7:c.*157_*168dup MANE Select	ENSP00000357873.3:n.*157_*168dup
ENST00000358776.6:c.*157_*168dup	ENSP00000357873.3:n.*157_*168dup
ENST00000368869.8:c.*157_*168dup	ENSP00000357862.4:n.*157_*168dup
NM_001609.3:c.*157_*168dup , LRG_451t1:c.*157_*168dup	NP_001600.1:n.*157_*168dup
NM_001330174.1:c.*157_*168dup	NP_001317103.1:n.*157_*168dup
NM_001330174.2:c.*157_*168dup	NP_001317103.1:n.*157_*168dup
NM_001609.4:c.*157_*168dup MANE Select	NP_001600.1:n.*157_*168dup
NM_001330174.3:c.*157_*168dup	NP_001317103.1:n.*157_*168dup