Canonical Allele Identifier: CA519345812
Gene: ABCD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.152991612G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153726157G>A , CM000685.2:g.153726157G>A GRCh38
NC_000023.10:g.152991612G>A , CM000685.1:g.152991612G>A GRCh37
NC_000023.9:g.152644806G>A NCBI36
NG_009022.2:g.6290G>A
NG_023231.1:g.3590C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.891G>A MANE Select ENSP00000218104.3:p.Gly297=
ENST00000218104.5:c.891G>A ENSP00000218104.3:p.Gly297=
ENST00000370129.4:c.336G>A ENSP00000359147.3:p.Gly112=
NM_000033.3:c.891G>A NP_000024.2:p.Gly297=
XR_938507.1:n.1307G>A
XR_938507.2:n.1307G>A
NM_000033.4:c.891G>A MANE Select NP_000024.2:p.Gly297=