Canonical Allele Identifier: CA1941711367

Gene: ACADSB

Linked Data

• dbSNP Id: rs1850373929

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123034693dup , CM000672.2:g.123034693dup	GRCh38
NC_000010.10:g.124794209dup , CM000672.1:g.124794209dup	GRCh37
NC_000010.9:g.124784199dup	NCBI36
NG_008003.1:g.30781dup , LRG_451:g.30781dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358776.7:c.202+178dup MANE Select	ENSP00000357873.3:n.202+178dup
ENST00000358776.6:c.202+178dup	ENSP00000357873.3:n.202+178dup
ENST00000368869.8:c.-4+178dup	ENSP00000357862.4:n.-4+178dup
ENST00000411816.2:n.219+178dup
NM_001609.3:c.202+178dup , LRG_451t1:c.202+178dup	NP_001600.1:n.202+178dup
NM_001330174.1:c.-4+178dup	NP_001317103.1:n.-4+178dup
NM_001330174.2:c.-4+178dup	NP_001317103.1:n.-4+178dup
NM_001609.4:c.202+178dup MANE Select	NP_001600.1:n.202+178dup
NM_001330174.3:c.-4+178dup	NP_001317103.1:n.-4+178dup