Canonical Allele Identifier: CA415104345
Gene: ABCD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 452524
dbSNP Id: rs1557054153

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153736111G>A , CM000685.2:g.153736111G>A GRCh38
NC_000023.10:g.153001565G>A , CM000685.1:g.153001565G>A GRCh37
NC_000023.9:g.152654759G>A NCBI36
NG_009022.2:g.16244G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1082-1G>A MANE Select ENSP00000218104.3:n.1082-1G>A
ENST00000218104.5:c.1082-1G>A ENSP00000218104.3:n.1082-1G>A
ENST00000443684.2:n.85-1G>A
NM_000033.3:c.1082-1G>A NP_000024.2:n.1082-1G>A
XR_938507.1:n.1498-1G>A
XR_938507.2:n.1498-1G>A
NM_000033.4:c.1082-1G>A MANE Select NP_000024.2:n.1082-1G>A