Canonical Allele Identifier: CA519345658
Gene: ABCD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.152991513G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153726058G>A , CM000685.2:g.153726058G>A GRCh38
NC_000023.10:g.152991513G>A , CM000685.1:g.152991513G>A GRCh37
NC_000023.9:g.152644707G>A NCBI36
NG_009022.2:g.6191G>A
NG_023231.1:g.3689C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.792G>A MANE Select ENSP00000218104.3:p.Lys264=
ENST00000218104.5:c.792G>A ENSP00000218104.3:p.Lys264=
ENST00000370129.4:c.237G>A ENSP00000359147.3:p.Lys79=
NM_000033.3:c.792G>A NP_000024.2:p.Lys264=
XR_938507.1:n.1208G>A
XR_938507.2:n.1208G>A
NM_000033.4:c.792G>A MANE Select NP_000024.2:p.Lys264=