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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA10550213
Gene: ABCD1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1686420
ClinVar RCV Id:
RCV002246933
RCV002391377
RCV003094045
dbSNP Id:
rs192525493
ExAC:
X:153002616 G / A
gnomAD v2:
X-153002616-G-A
gnomAD v3:
X-153737162-G-A
gnomAD v4:
X-153737162-G-A
MyVariant Identifiers:
chrX:g.153002616G>A (hg19)
chrX:g.153737162G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.153737162G>A , CM000685.2:g.153737162G>A
GRCh38
NC_000023.10:g.153002616G>A , CM000685.1:g.153002616G>A
GRCh37
NC_000023.9:g.152655810G>A
NCBI36
NG_009022.2:g.17295G>A
Transcript Alleles
HGVS
Amino-acid change
ENST00000218104.6:c.1399G>A
MANE Select
ENSP00000218104.3:p.Val467Met
ENST00000218104.5:c.1399G>A
ENSP00000218104.3:p.Val467Met
ENST00000443684.2:n.402G>A
NM_000033.3:c.1399G>A
NP_000024.2:p.Val467Met
XR_938507.1:n.1871G>A
XR_938507.2:n.1871G>A
NM_000033.4:c.1399G>A
MANE Select
NP_000024.2:p.Val467Met
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