Canonical Allele Identifier: CA645288087
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs1173914716
MyVariant Identifiers: chrX:g.153001759T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153736305T>G , CM000685.2:g.153736305T>G GRCh38
NC_000023.10:g.153001759T>G , CM000685.1:g.153001759T>G GRCh37
NC_000023.9:g.152654953T>G NCBI36
NG_009022.2:g.16438T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1225-40T>G MANE Select ENSP00000218104.3:n.1225-40T>G
ENST00000218104.5:c.1225-40T>G ENSP00000218104.3:n.1225-40T>G
ENST00000443684.2:n.228-40T>G
NM_000033.3:c.1225-40T>G NP_000024.2:n.1225-40T>G
XR_938507.1:n.1641-40T>G
XR_938507.2:n.1641-40T>G
NM_000033.4:c.1225-40T>G MANE Select NP_000024.2:n.1225-40T>G