Canonical Allele Identifier: CA415115602
Gene: ABCD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153008441G>A (hg19) chrX:g.153742987G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153742987G>A , CM000685.2:g.153742987G>A GRCh38
NC_000023.10:g.153008441G>A , CM000685.1:g.153008441G>A GRCh37
NC_000023.9:g.152661635G>A NCBI36
NG_009022.2:g.23120G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1781G>A MANE Select ENSP00000218104.3:p.Gly594Asp
ENST00000218104.5:c.1781G>A ENSP00000218104.3:p.Gly594Asp
NM_000033.3:c.1781G>A NP_000024.2:p.Gly594Asp
XR_938507.1:n.2253G>A
XR_938507.2:n.2253G>A
NM_000033.4:c.1781G>A MANE Select NP_000024.2:p.Gly594Asp
Search 100 bp 5'
Search 100 bp 3'