Canonical Allele Identifier: CA471754526

Gene: ACADSB

Linked Data

• MyVariant Identifiers: chr10:g.124793994A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123034478A>G , CM000672.2:g.123034478A>G	GRCh38
NC_000010.10:g.124793994A>G , CM000672.1:g.124793994A>G	GRCh37
NC_000010.9:g.124783984A>G	NCBI36
NG_008003.1:g.30566A>G , LRG_451:g.30566A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358776.7:c.165A>G MANE Select	ENSP00000357873.3:p.Gln55=
ENST00000358776.6:c.165A>G	ENSP00000357873.3:p.Gln55=
ENST00000368869.8:c.-41A>G	ENSP00000357862.4:n.-41A>G
ENST00000411816.2:n.182A>G
NM_001609.3:c.165A>G , LRG_451t1:c.165A>G	NP_001600.1:p.Gln55=
NM_001330174.1:c.-41A>G	NP_001317103.1:n.-41A>G
NM_001330174.2:c.-41A>G	NP_001317103.1:n.-41A>G
NM_001609.4:c.165A>G MANE Select	NP_001600.1:p.Gln55=
NM_001330174.3:c.-41A>G	NP_001317103.1:n.-41A>G