Canonical Allele Identifier: CA415111426
Gene: ABCD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153005618G>A (hg19) chrX:g.153740164G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153740164G>A , CM000685.2:g.153740164G>A GRCh38
NC_000023.10:g.153005618G>A , CM000685.1:g.153005618G>A GRCh37
NC_000023.9:g.152658812G>A NCBI36
NG_009022.2:g.20297G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1561G>A MANE Select ENSP00000218104.3:p.Gly521Ser
ENST00000218104.5:c.1561G>A ENSP00000218104.3:p.Gly521Ser
ENST00000443684.2:n.564G>A
NM_000033.3:c.1561G>A NP_000024.2:p.Gly521Ser
XR_938507.1:n.2033G>A
XR_938507.2:n.2033G>A
NM_000033.4:c.1561G>A MANE Select NP_000024.2:p.Gly521Ser
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