Canonical Allele Identifier: CA2466456628
Gene: ABCD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153740685C= , CM000685.2:g.153740685C= GRCh38
NC_000023.10:g.153006139C= , CM000685.1:g.153006139C= GRCh37
NC_000023.9:g.152659333C= NCBI36
NG_009022.2:g.20818C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1746C= MANE Select ENSP00000218104.3:p.Val582=
ENST00000218104.5:c.1746C= ENSP00000218104.3:p.Val582=
NM_000033.3:c.1746C= NP_000024.2:p.Val582=
XR_938507.1:n.2218C=
XR_938507.2:n.2218C=
NM_000033.4:c.1746C= MANE Select NP_000024.2:p.Val582=