Canonical Allele Identifier: CA415098851
Gene: ABCD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.152991158T>A (hg19) chrX:g.153725703T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153725703T>A , CM000685.2:g.153725703T>A GRCh38
NC_000023.10:g.152991158T>A , CM000685.1:g.152991158T>A GRCh37
NC_000023.9:g.152644352T>A NCBI36
NG_009022.2:g.5836T>A
NG_023231.1:g.4044A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.437T>A MANE Select ENSP00000218104.3:p.Phe146Tyr
ENST00000218104.5:c.437T>A ENSP00000218104.3:p.Phe146Tyr
NM_000033.3:c.437T>A NP_000024.2:p.Phe146Tyr
XR_938507.1:n.853T>A
XR_938507.2:n.853T>A
NM_000033.4:c.437T>A MANE Select NP_000024.2:p.Phe146Tyr
Search 100 bp 5'
Search 100 bp 3'