Canonical Allele Identifier: CA15018196
Gene: ABCD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1293829
ClinVar RCV Id: RCV001718410
dbSNP Id: rs11156606

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153741041A>C , CM000685.2:g.153741041A>C GRCh38
NC_000023.10:g.153006495A>C , CM000685.1:g.153006495A>C GRCh37
NC_000023.9:g.152659689A>C NCBI36
NG_009022.2:g.21174A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1780+322A>C MANE Select ENSP00000218104.3:n.1780+322A>C
ENST00000218104.5:c.1780+322A>C ENSP00000218104.3:n.1780+322A>C
NM_000033.3:c.1780+322A>C NP_000024.2:n.1780+322A>C
XR_938507.1:n.2252+322A>C
XR_938507.2:n.2252+322A>C
NM_000033.4:c.1780+322A>C MANE Select NP_000024.2:n.1780+322A>C