Canonical Allele Identifier: CA415100366
Gene: ABCD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153726161C>A , CM000685.2:g.153726161C>A GRCh38
NC_000023.10:g.152991616C>A , CM000685.1:g.152991616C>A GRCh37
NC_000023.9:g.152644810C>A NCBI36
NG_009022.2:g.6294C>A
NG_023231.1:g.3586G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.895C>A MANE Select ENSP00000218104.3:p.His299Asn
ENST00000218104.5:c.895C>A ENSP00000218104.3:p.His299Asn
ENST00000370129.4:c.340C>A ENSP00000359147.3:p.His114Asn
NM_000033.3:c.895C>A NP_000024.2:p.His299Asn
XR_938507.1:n.1311C>A
XR_938507.2:n.1311C>A
NM_000033.4:c.895C>A MANE Select NP_000024.2:p.His299Asn