Canonical Allele Identifier: CA519345927

Gene: ABCD1

Linked Data

• MyVariant Identifiers: chrX:g.153001936T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153736482T>C , CM000685.2:g.153736482T>C	GRCh38
NC_000023.10:g.153001936T>C , CM000685.1:g.153001936T>C	GRCh37
NC_000023.9:g.152655130T>C	NCBI36
NG_009022.2:g.16615T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218104.6:c.1362T>C MANE Select	ENSP00000218104.3:p.Gly454=
ENST00000218104.5:c.1362T>C	ENSP00000218104.3:p.Gly454=
ENST00000443684.2:n.365T>C
NM_000033.3:c.1362T>C	NP_000024.2:p.Gly454=
XR_938507.1:n.1778T>C
XR_938507.2:n.1778T>C
NM_000033.4:c.1362T>C MANE Select	NP_000024.2:p.Gly454=