Canonical Allele Identifier: CA2580612512
Gene: ABCD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2438766
ClinVar RCV Id: RCV003139518

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153740189_153740191del , CM000685.2:g.153740189_153740191del GRCh38
NC_000023.10:g.153005643_153005645del , CM000685.1:g.153005643_153005645del GRCh37
NC_000023.9:g.152658837_152658839del NCBI36
NG_009022.2:g.20322_20324del

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1586_1588del MANE Select ENSP00000218104.3:p.Gly529del
ENST00000218104.5:c.1586_1588del ENSP00000218104.3:p.Gly529del
ENST00000443684.2:n.589_591del
NM_000033.3:c.1586_1588del NP_000024.2:p.Gly529del
XR_938507.1:n.2058_2060del
XR_938507.2:n.2058_2060del
NM_000033.4:c.1586_1588del MANE Select NP_000024.2:p.Gly529del