Canonical Allele Identifier: CA2466456747
Gene: ABCD1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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