Canonical Allele Identifier: CA415116980

Gene: ABCD1

Linked Data

• MyVariant Identifiers: chrX:g.153008722A>T (hg19) ; chrX:g.153743268A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153743268A>T , CM000685.2:g.153743268A>T	GRCh38
NC_000023.10:g.153008722A>T , CM000685.1:g.153008722A>T	GRCh37
NC_000023.9:g.152661916A>T	NCBI36
NG_009022.2:g.23401A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218104.6:c.1913A>T MANE Select	ENSP00000218104.3:p.Asp638Val
ENST00000218104.5:c.1913A>T	ENSP00000218104.3:p.Asp638Val
NM_000033.3:c.1913A>T	NP_000024.2:p.Asp638Val
XR_938507.1:n.2385A>T
XR_938507.2:n.2385A>T
NM_000033.4:c.1913A>T MANE Select	NP_000024.2:p.Asp638Val