Canonical Allele Identifier: CA415106627
Gene: ABCD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153001874T>C (hg19) chrX:g.153736420T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153736420T>C , CM000685.2:g.153736420T>C GRCh38
NC_000023.10:g.153001874T>C , CM000685.1:g.153001874T>C GRCh37
NC_000023.9:g.152655068T>C NCBI36
NG_009022.2:g.16553T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1300T>C MANE Select ENSP00000218104.3:p.Phe434Leu
ENST00000218104.5:c.1300T>C ENSP00000218104.3:p.Phe434Leu
ENST00000443684.2:n.303T>C
NM_000033.3:c.1300T>C NP_000024.2:p.Phe434Leu
XR_938507.1:n.1716T>C
XR_938507.2:n.1716T>C
NM_000033.4:c.1300T>C MANE Select NP_000024.2:p.Phe434Leu
Search 100 bp 5'
Search 100 bp 3'