Canonical Allele Identifier: CA2602662104
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs2148399152

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153743187G>A , CM000685.2:g.153743187G>A GRCh38
NC_000023.10:g.153008641G>A , CM000685.1:g.153008641G>A GRCh37
NC_000023.9:g.152661835G>A NCBI36
NG_009022.2:g.23320G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1866-34G>A MANE Select ENSP00000218104.3:n.1866-34G>A
ENST00000218104.5:c.1866-34G>A ENSP00000218104.3:n.1866-34G>A
NM_000033.3:c.1866-34G>A NP_000024.2:n.1866-34G>A
XR_938507.1:n.2338-34G>A
XR_938507.2:n.2338-34G>A
NM_000033.4:c.1866-34G>A MANE Select NP_000024.2:n.1866-34G>A