Canonical Allele Identifier: CA873266339
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs1490500344
gnomAD v3: X-153736059-G-A
gnomAD v4: X-153736059-G-A
MyVariant Identifiers: chrX:g.153736059G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153736059G>A , CM000685.2:g.153736059G>A GRCh38
NC_000023.10:g.153001513G>A , CM000685.1:g.153001513G>A GRCh37
NC_000023.9:g.152654707G>A NCBI36
NG_009022.2:g.16192G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1082-53G>A MANE Select ENSP00000218104.3:n.1082-53G>A
ENST00000218104.5:c.1082-53G>A ENSP00000218104.3:n.1082-53G>A
ENST00000443684.2:n.85-53G>A
NM_000033.3:c.1082-53G>A NP_000024.2:n.1082-53G>A
XR_938507.1:n.1498-53G>A
XR_938507.2:n.1498-53G>A
NM_000033.4:c.1082-53G>A MANE Select NP_000024.2:n.1082-53G>A
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