Canonical Allele Identifier: CA415098846

Gene: ABCD1

Linked Data

• MyVariant Identifiers: chrX:g.152991154A>T (hg19) ; chrX:g.153725699A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153725699A>T , CM000685.2:g.153725699A>T	GRCh38
NC_000023.10:g.152991154A>T , CM000685.1:g.152991154A>T	GRCh37
NC_000023.9:g.152644348A>T	NCBI36
NG_009022.2:g.5832A>T
NG_023231.1:g.4048T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000218104.6:c.433A>T MANE Select	ENSP00000218104.3:p.Thr145Ser
ENST00000218104.5:c.433A>T	ENSP00000218104.3:p.Thr145Ser
NM_000033.3:c.433A>T	NP_000024.2:p.Thr145Ser
XR_938507.1:n.849A>T
XR_938507.2:n.849A>T
NM_000033.4:c.433A>T MANE Select	NP_000024.2:p.Thr145Ser