Canonical Allele Identifier: CA645288140
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs1557055282
gnomAD v2: X-153008566-A-G
gnomAD v4: X-153743112-A-G
MyVariant Identifiers: chrX:g.153008566A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153743112A>G , CM000685.2:g.153743112A>G GRCh38
NC_000023.10:g.153008566A>G , CM000685.1:g.153008566A>G GRCh37
NC_000023.9:g.152661760A>G NCBI36
NG_009022.2:g.23245A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1865+41A>G MANE Select ENSP00000218104.3:n.1865+41A>G
ENST00000218104.5:c.1865+41A>G ENSP00000218104.3:n.1865+41A>G
NM_000033.3:c.1865+41A>G NP_000024.2:n.1865+41A>G
XR_938507.1:n.2337+41A>G
XR_938507.2:n.2337+41A>G
NM_000033.4:c.1865+41A>G MANE Select NP_000024.2:n.1865+41A>G
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