Canonical Allele Identifier: CA519231315
Gene: ABCD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153008747G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153743293G>T , CM000685.2:g.153743293G>T GRCh38
NC_000023.10:g.153008747G>T , CM000685.1:g.153008747G>T GRCh37
NC_000023.9:g.152661941G>T NCBI36
NG_009022.2:g.23426G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1938G>T MANE Select ENSP00000218104.3:p.Ala646=
ENST00000218104.5:c.1938G>T ENSP00000218104.3:p.Ala646=
NM_000033.3:c.1938G>T NP_000024.2:p.Ala646=
XR_938507.1:n.2410G>T
XR_938507.2:n.2410G>T
NM_000033.4:c.1938G>T MANE Select NP_000024.2:p.Ala646=