Canonical Allele Identifier: CA1941711356

Gene: ACADSB

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123034678_123034682delinsAATTG , CM000672.2:g.123034678_123034682delinsAATTG	GRCh38
NC_000010.10:g.124794194_124794198delinsAATTG , CM000672.1:g.124794194_124794198delinsAATTG	GRCh37
NC_000010.9:g.124784184_124784188delinsAATTG	NCBI36
NG_008003.1:g.30766_30770delinsAATTG , LRG_451:g.30766_30770delinsAATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358776.7:c.202+163_202+167delinsAATTG MANE Select	ENSP00000357873.3:n.202+163_202+167delinsAATTG
ENST00000358776.6:c.202+163_202+167delinsAATTG	ENSP00000357873.3:n.202+163_202+167delinsAATTG
ENST00000368869.8:c.-4+163_-4+167delinsAATTG	ENSP00000357862.4:n.-4+163_-4+167delinsAATTG
ENST00000411816.2:n.219+163_219+167delinsAATTG
NM_001609.3:c.202+163_202+167delinsAATTG , LRG_451t1:c.202+163_202+167delinsAATTG	NP_001600.1:n.202+163_202+167delinsAATTG
NM_001330174.1:c.-4+163_-4+167delinsAATTG	NP_001317103.1:n.-4+163_-4+167delinsAATTG
NM_001330174.2:c.-4+163_-4+167delinsAATTG	NP_001317103.1:n.-4+163_-4+167delinsAATTG
NM_001609.4:c.202+163_202+167delinsAATTG MANE Select	NP_001600.1:n.202+163_202+167delinsAATTG
NM_001330174.3:c.-4+163_-4+167delinsAATTG	NP_001317103.1:n.-4+163_-4+167delinsAATTG