Canonical Allele Identifier: CA415111754

Gene: ABCD1

Linked Data

• MyVariant Identifiers: chrX:g.153005655A>T (hg19) ; chrX:g.153740201A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153740201A>T , CM000685.2:g.153740201A>T	GRCh38
NC_000023.10:g.153005655A>T , CM000685.1:g.153005655A>T	GRCh37
NC_000023.9:g.152658849A>T	NCBI36
NG_009022.2:g.20334A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218104.6:c.1598A>T MANE Select	ENSP00000218104.3:p.Lys533Met
ENST00000218104.5:c.1598A>T	ENSP00000218104.3:p.Lys533Met
ENST00000443684.2:n.601A>T
NM_000033.3:c.1598A>T	NP_000024.2:p.Lys533Met
XR_938507.1:n.2070A>T
XR_938507.2:n.2070A>T
NM_000033.4:c.1598A>T MANE Select	NP_000024.2:p.Lys533Met