Canonical Allele Identifier: CA645288158
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs1160989768
gnomAD v2: X-153008314-C-CA
gnomAD v3: X-153742860-C-CA
gnomAD v4: X-153742860-C-CA
MyVariant Identifiers: chrX:g.153008314_153008315insA (hg19) chrX:g.153742860_153742861insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153742862dup , CM000685.2:g.153742862dup GRCh38
NC_000023.10:g.153008316dup , CM000685.1:g.153008316dup GRCh37
NC_000023.9:g.152661510dup NCBI36
NG_009022.2:g.22995dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1781-125dup MANE Select ENSP00000218104.3:n.1781-125dup
ENST00000218104.5:c.1781-125dup ENSP00000218104.3:n.1781-125dup
NM_000033.3:c.1781-125dup NP_000024.2:n.1781-125dup
XR_938507.1:n.2253-125dup
XR_938507.2:n.2253-125dup
NM_000033.4:c.1781-125dup MANE Select NP_000024.2:n.1781-125dup
Search 100 bp 5'
Search 100 bp 3'