Canonical Allele Identifier: CA519229986
Gene: ABCD1 HGNC NCBI

Linked Data

gnomAD v4: X-153742997-T-A
MyVariant Identifiers: chrX:g.153008451T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153742997T>A , CM000685.2:g.153742997T>A GRCh38
NC_000023.10:g.153008451T>A , CM000685.1:g.153008451T>A GRCh37
NC_000023.9:g.152661645T>A NCBI36
NG_009022.2:g.23130T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1791T>A MANE Select ENSP00000218104.3:p.Ala597=
ENST00000218104.5:c.1791T>A ENSP00000218104.3:p.Ala597=
NM_000033.3:c.1791T>A NP_000024.2:p.Ala597=
XR_938507.1:n.2263T>A
XR_938507.2:n.2263T>A
NM_000033.4:c.1791T>A MANE Select NP_000024.2:p.Ala597=
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Search 100 bp 3'