Canonical Allele Identifier: CA645160459
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs1557054294
gnomAD v2: X-153002544-T-TCCCCA
gnomAD v3: X-153737090-T-TCCCCA
gnomAD v4: X-153737090-T-TCCCCA
MyVariant Identifiers: chrX:g.153002544_153002545insCCCCA (hg19) chrX:g.153737090_153737091insCCCCA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153737091_153737095dup , CM000685.2:g.153737091_153737095dup GRCh38
NC_000023.10:g.153002545_153002549dup , CM000685.1:g.153002545_153002549dup GRCh37
NC_000023.9:g.152655739_152655743dup NCBI36
NG_009022.2:g.17224_17228dup

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1394-66_1394-62dup MANE Select ENSP00000218104.3:n.1394-66_1394-62dup
ENST00000218104.5:c.1394-66_1394-62dup ENSP00000218104.3:n.1394-66_1394-62dup
ENST00000443684.2:n.397-66_397-62dup
NM_000033.3:c.1394-66_1394-62dup NP_000024.2:n.1394-66_1394-62dup
XR_938507.1:n.1866-66_1866-62dup
XR_938507.2:n.1866-66_1866-62dup
NM_000033.4:c.1394-66_1394-62dup MANE Select NP_000024.2:n.1394-66_1394-62dup
Search 100 bp 5'
Search 100 bp 3'