Canonical Allele Identifier: CA2580612507
Gene: ABCD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2503475
ClinVar RCV Id: RCV003230247

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153736156del , CM000685.2:g.153736156del GRCh38
NC_000023.10:g.153001610del , CM000685.1:g.153001610del GRCh37
NC_000023.9:g.152654804del NCBI36
NG_009022.2:g.16289del

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1126del MANE Select ENSP00000218104.3:p.Glu376SerfsTer3
ENST00000218104.5:c.1126del ENSP00000218104.3:p.Glu376SerfsTer3
ENST00000443684.2:n.129del
NM_000033.3:c.1126del NP_000024.2:p.Glu376SerfsTer3
XR_938507.1:n.1542del
XR_938507.2:n.1542del
NM_000033.4:c.1126del MANE Select NP_000024.2:p.Glu376SerfsTer3