Canonical Allele Identifier: CA519218051

Gene: ABCD1

Linked Data

• MyVariant Identifiers: chrX:g.153002618G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153737164G>T , CM000685.2:g.153737164G>T	GRCh38
NC_000023.10:g.153002618G>T , CM000685.1:g.153002618G>T	GRCh37
NC_000023.9:g.152655812G>T	NCBI36
NG_009022.2:g.17297G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218104.6:c.1401G>T MANE Select	ENSP00000218104.3:p.Val467=
ENST00000218104.5:c.1401G>T	ENSP00000218104.3:p.Val467=
ENST00000443684.2:n.404G>T
NM_000033.3:c.1401G>T	NP_000024.2:p.Val467=
XR_938507.1:n.1873G>T
XR_938507.2:n.1873G>T
NM_000033.4:c.1401G>T MANE Select	NP_000024.2:p.Val467=