Canonical Allele Identifier: CA415099058
Gene: ABCD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.152991256A>C (hg19) chrX:g.153725801A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153725801A>C , CM000685.2:g.153725801A>C GRCh38
NC_000023.10:g.152991256A>C , CM000685.1:g.152991256A>C GRCh37
NC_000023.9:g.152644450A>C NCBI36
NG_009022.2:g.5934A>C
NG_023231.1:g.3946T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.535A>C MANE Select ENSP00000218104.3:p.Thr179Pro
ENST00000218104.5:c.535A>C ENSP00000218104.3:p.Thr179Pro
NM_000033.3:c.535A>C NP_000024.2:p.Thr179Pro
XR_938507.1:n.951A>C
XR_938507.2:n.951A>C
NM_000033.4:c.535A>C MANE Select NP_000024.2:p.Thr179Pro
Search 100 bp 5'
Search 100 bp 3'