Canonical Allele Identifier: CA415105230
Gene: ABCD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153001654C>A (hg19) chrX:g.153736200C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153736200C>A , CM000685.2:g.153736200C>A GRCh38
NC_000023.10:g.153001654C>A , CM000685.1:g.153001654C>A GRCh37
NC_000023.9:g.152654848C>A NCBI36
NG_009022.2:g.16333C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1170C>A MANE Select ENSP00000218104.3:p.Asn390Lys
ENST00000218104.5:c.1170C>A ENSP00000218104.3:p.Asn390Lys
ENST00000443684.2:n.173C>A
NM_000033.3:c.1170C>A NP_000024.2:p.Asn390Lys
XR_938507.1:n.1586C>A
XR_938507.2:n.1586C>A
NM_000033.4:c.1170C>A MANE Select NP_000024.2:p.Asn390Lys
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