Canonical Allele Identifier: CA645161000

Gene: ABCD1

Linked Data

• dbSNP Id: rs1557054813
• gnomAD v2: X-153005917-AGCGTGTGGAT-A
• gnomAD v3: X-153740463-AGCGTGTGGAT-A
• gnomAD v4: X-153740463-AGCGTGTGGAT-A
• MyVariant Identifiers: chrX:g.153005918_153005927del (hg19) ; chrX:g.153740464_153740473del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153740471_153740480del , CM000685.2:g.153740471_153740480del	GRCh38
NC_000023.10:g.153005925_153005934del , CM000685.1:g.153005925_153005934del	GRCh37
NC_000023.9:g.152659119_152659128del	NCBI36
NG_009022.2:g.20604_20613del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218104.6:c.1635-103_1635-94del MANE Select	ENSP00000218104.3:n.1635-103_1635-94del
ENST00000218104.5:c.1635-103_1635-94del	ENSP00000218104.3:n.1635-103_1635-94del
ENST00000443684.2:n.638-103_638-94del
NM_000033.3:c.1635-103_1635-94del	NP_000024.2:n.1635-103_1635-94del
XR_938507.1:n.2107-103_2107-94del
XR_938507.2:n.2107-103_2107-94del
NM_000033.4:c.1635-103_1635-94del MANE Select	NP_000024.2:n.1635-103_1635-94del