Canonical Allele Identifier: CA2466451025
Gene: ABCD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153725702T= , CM000685.2:g.153725702T= GRCh38
NC_000023.10:g.152991157T= , CM000685.1:g.152991157T= GRCh37
NC_000023.9:g.152644351T= NCBI36
NG_009022.2:g.5835T=
NG_023231.1:g.4045A=

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.436T= MANE Select ENSP00000218104.3:p.Phe146=
ENST00000218104.5:c.436T= ENSP00000218104.3:p.Phe146=
NM_000033.3:c.436T= NP_000024.2:p.Phe146=
XR_938507.1:n.852T=
XR_938507.2:n.852T=
NM_000033.4:c.436T= MANE Select NP_000024.2:p.Phe146=