Canonical Allele Identifier: CA2580617840
Gene: ABCD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2579950
ClinVar RCV Id: RCV003328925

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153743062_153743088del , CM000685.2:g.153743062_153743088del GRCh38
NC_000023.10:g.153008516_153008542del , CM000685.1:g.153008516_153008542del GRCh37
NC_000023.9:g.152661710_152661736del NCBI36
NG_009022.2:g.23195_23221del

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1856_1865+17del
ENST00000218104.5:c.1856_1865+17del
NM_000033.3:c.1856_1865+17del
XR_938507.1:n.2328_2337+17del
XR_938507.2:n.2328_2337+17del
NM_000033.4:c.1856_1865+17del