Canonical Allele Identifier: CA415117492

Gene: ABCD1

Linked Data

• MyVariant Identifiers: chrX:g.153008760G>C (hg19) ; chrX:g.153743306G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153743306G>C , CM000685.2:g.153743306G>C	GRCh38
NC_000023.10:g.153008760G>C , CM000685.1:g.153008760G>C	GRCh37
NC_000023.9:g.152661954G>C	NCBI36
NG_009022.2:g.23439G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218104.6:c.1951G>C MANE Select	ENSP00000218104.3:p.Gly651Arg
ENST00000218104.5:c.1951G>C	ENSP00000218104.3:p.Gly651Arg
NM_000033.3:c.1951G>C	NP_000024.2:p.Gly651Arg
XR_938507.1:n.2423G>C
XR_938507.2:n.2423G>C
NM_000033.4:c.1951G>C MANE Select	NP_000024.2:p.Gly651Arg