Canonical Allele Identifier: CA1941716764

Gene: ACADSB

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123056931C= , CM000672.2:g.123056931C=	GRCh38
NC_000010.10:g.124816447C= , CM000672.1:g.124816447C=	GRCh37
NC_000010.9:g.124806437C=	NCBI36
NG_008003.1:g.53019C= , LRG_451:g.53019C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000358776.7:c.*3166C= MANE Select	ENSP00000357873.3:n.*3166C=
ENST00000358776.6:c.*3166C=	ENSP00000357873.3:n.*3166C=
NM_001609.3:c.*3166C= , LRG_451t1:c.*3166C=	NP_001600.1:n.*3166C=
NM_001330174.1:c.*3166C=	NP_001317103.1:n.*3166C=
NM_001330174.2:c.*3166C=	NP_001317103.1:n.*3166C=
NM_001609.4:c.*3166C= MANE Select	NP_001600.1:n.*3166C=
NM_001330174.3:c.*3166C=	NP_001317103.1:n.*3166C=