Canonical Allele Identifier: CA415111664
Gene: ABCD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153005646T>A (hg19) chrX:g.153740192T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153740192T>A , CM000685.2:g.153740192T>A GRCh38
NC_000023.10:g.153005646T>A , CM000685.1:g.153005646T>A GRCh37
NC_000023.9:g.152658840T>A NCBI36
NG_009022.2:g.20325T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1589T>A MANE Select ENSP00000218104.3:p.Val530Glu
ENST00000218104.5:c.1589T>A ENSP00000218104.3:p.Val530Glu
ENST00000443684.2:n.592T>A
NM_000033.3:c.1589T>A NP_000024.2:p.Val530Glu
XR_938507.1:n.2061T>A
XR_938507.2:n.2061T>A
NM_000033.4:c.1589T>A MANE Select NP_000024.2:p.Val530Glu
Search 100 bp 5'
Search 100 bp 3'