Canonical Allele Identifier: CA2611278152

Gene: ACADSB

Linked Data

• gnomAD v4: 10-123034639-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123034640del , CM000672.2:g.123034640del	GRCh38
NC_000010.10:g.124794156del , CM000672.1:g.124794156del	GRCh37
NC_000010.9:g.124784146del	NCBI36
NG_008003.1:g.30728del , LRG_451:g.30728del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358776.7:c.202+125del MANE Select	ENSP00000357873.3:n.202+125del
ENST00000358776.6:c.202+125del	ENSP00000357873.3:n.202+125del
ENST00000368869.8:c.-4+125del	ENSP00000357862.4:n.-4+125del
ENST00000411816.2:n.219+125del
NM_001609.3:c.202+125del , LRG_451t1:c.202+125del	NP_001600.1:n.202+125del
NM_001330174.1:c.-4+125del	NP_001317103.1:n.-4+125del
NM_001330174.2:c.-4+125del	NP_001317103.1:n.-4+125del
NM_001609.4:c.202+125del MANE Select	NP_001600.1:n.202+125del
NM_001330174.3:c.-4+125del	NP_001317103.1:n.-4+125del