Canonical Allele Identifier: CA378615780

Gene: ACADSB

Linked Data

• MyVariant Identifiers: chr10:g.124793929A>T (hg19) ; chr10:g.123034413A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123034413A>T , CM000672.2:g.123034413A>T	GRCh38
NC_000010.10:g.124793929A>T , CM000672.1:g.124793929A>T	GRCh37
NC_000010.9:g.124783919A>T	NCBI36
NG_008003.1:g.30501A>T , LRG_451:g.30501A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358776.7:c.100A>T MANE Select	ENSP00000357873.3:p.Lys34Ter
ENST00000358776.6:c.100A>T	ENSP00000357873.3:p.Lys34Ter
ENST00000368869.8:c.-106A>T	ENSP00000357862.4:n.-106A>T
ENST00000411816.2:n.117A>T
NM_001609.3:c.100A>T , LRG_451t1:c.100A>T	NP_001600.1:p.Lys34Ter
NM_001330174.1:c.-106A>T	NP_001317103.1:n.-106A>T
NM_001330174.2:c.-106A>T	NP_001317103.1:n.-106A>T
NM_001609.4:c.100A>T MANE Select	NP_001600.1:p.Lys34Ter
NM_001330174.3:c.-106A>T	NP_001317103.1:n.-106A>T