Canonical Allele Identifier: CA519345548
Gene: ABCD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.152991144C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153725689C>A , CM000685.2:g.153725689C>A GRCh38
NC_000023.10:g.152991144C>A , CM000685.1:g.152991144C>A GRCh37
NC_000023.9:g.152644338C>A NCBI36
NG_009022.2:g.5822C>A
NG_023231.1:g.4058G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.423C>A MANE Select ENSP00000218104.3:p.Ala141=
ENST00000218104.5:c.423C>A ENSP00000218104.3:p.Ala141=
NM_000033.3:c.423C>A NP_000024.2:p.Ala141=
XR_938507.1:n.839C>A
XR_938507.2:n.839C>A
NM_000033.4:c.423C>A MANE Select NP_000024.2:p.Ala141=
Search 100 bp 5'
Search 100 bp 3'