Canonical Allele Identifier: CA415117129
Gene: ABCD1 HGNC NCBI

Linked Data

dbSNP Id: rs1417326617
gnomAD v2: X-153008735-G-T
gnomAD v4: X-153743281-G-T
MyVariant Identifiers: chrX:g.153008735G>T (hg19) chrX:g.153743281G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153743281G>T , CM000685.2:g.153743281G>T GRCh38
NC_000023.10:g.153008735G>T , CM000685.1:g.153008735G>T GRCh37
NC_000023.9:g.152661929G>T NCBI36
NG_009022.2:g.23414G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1926G>T MANE Select ENSP00000218104.3:p.Lys642Asn
ENST00000218104.5:c.1926G>T ENSP00000218104.3:p.Lys642Asn
NM_000033.3:c.1926G>T NP_000024.2:p.Lys642Asn
XR_938507.1:n.2398G>T
XR_938507.2:n.2398G>T
NM_000033.4:c.1926G>T MANE Select NP_000024.2:p.Lys642Asn
Search 100 bp 5'
Search 100 bp 3'