Canonical Allele Identifier: CA2466451018
Gene: ABCD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153725687G= , CM000685.2:g.153725687G= GRCh38
NC_000023.10:g.152991142G= , CM000685.1:g.152991142G= GRCh37
NC_000023.9:g.152644336G= NCBI36
NG_009022.2:g.5820G=
NG_023231.1:g.4060C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.421G= MANE Select ENSP00000218104.3:p.Ala141=
ENST00000218104.5:c.421G= ENSP00000218104.3:p.Ala141=
NM_000033.3:c.421G= NP_000024.2:p.Ala141=
XR_938507.1:n.837G=
XR_938507.2:n.837G=
NM_000033.4:c.421G= MANE Select NP_000024.2:p.Ala141=