Canonical Allele Identifier: CA1941711304

Gene: ACADSB

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123034539_123034540delinsCT , CM000672.2:g.123034539_123034540delinsCT	GRCh38
NC_000010.10:g.124794055_124794056delinsCT , CM000672.1:g.124794055_124794056delinsCT	GRCh37
NC_000010.9:g.124784045_124784046delinsCT	NCBI36
NG_008003.1:g.30627_30628delinsCT , LRG_451:g.30627_30628delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358776.7:c.202+24_202+25delinsCT MANE Select	ENSP00000357873.3:n.202+24_202+25delinsCT
ENST00000358776.6:c.202+24_202+25delinsCT	ENSP00000357873.3:n.202+24_202+25delinsCT
ENST00000368869.8:c.-4+24_-4+25delinsCT	ENSP00000357862.4:n.-4+24_-4+25delinsCT
ENST00000411816.2:n.219+24_219+25delinsCT
NM_001609.3:c.202+24_202+25delinsCT , LRG_451t1:c.202+24_202+25delinsCT	NP_001600.1:n.202+24_202+25delinsCT
NM_001330174.1:c.-4+24_-4+25delinsCT	NP_001317103.1:n.-4+24_-4+25delinsCT
NM_001330174.2:c.-4+24_-4+25delinsCT	NP_001317103.1:n.-4+24_-4+25delinsCT
NM_001609.4:c.202+24_202+25delinsCT MANE Select	NP_001600.1:n.202+24_202+25delinsCT
NM_001330174.3:c.-4+24_-4+25delinsCT	NP_001317103.1:n.-4+24_-4+25delinsCT