Canonical Allele Identifier: CA378615569

Gene: ACADSB

Linked Data

• MyVariant Identifiers: chr10:g.124793871G>T (hg19) ; chr10:g.123034355G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123034355G>T , CM000672.2:g.123034355G>T	GRCh38
NC_000010.10:g.124793871G>T , CM000672.1:g.124793871G>T	GRCh37
NC_000010.9:g.124783861G>T	NCBI36
NG_008003.1:g.30443G>T , LRG_451:g.30443G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358776.7:c.43-1G>T MANE Select	ENSP00000357873.3:n.43-1G>T
ENST00000358776.6:c.43-1G>T	ENSP00000357873.3:n.43-1G>T
ENST00000368869.8:c.-163-1G>T	ENSP00000357862.4:n.-163-1G>T
ENST00000411816.2:n.60-1G>T
NM_001609.3:c.43-1G>T , LRG_451t1:c.43-1G>T	NP_001600.1:n.43-1G>T
NM_001330174.1:c.-163-1G>T	NP_001317103.1:n.-163-1G>T
NM_001330174.2:c.-163-1G>T	NP_001317103.1:n.-163-1G>T
NM_001609.4:c.43-1G>T MANE Select	NP_001600.1:n.43-1G>T
NM_001330174.3:c.-163-1G>T	NP_001317103.1:n.-163-1G>T