Canonical Allele Identifier: CA415111383
Gene: ABCD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153005612A>T (hg19) chrX:g.153740158A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153740158A>T , CM000685.2:g.153740158A>T GRCh38
NC_000023.10:g.153005612A>T , CM000685.1:g.153005612A>T GRCh37
NC_000023.9:g.152658806A>T NCBI36
NG_009022.2:g.20291A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1555A>T MANE Select ENSP00000218104.3:p.Ile519Phe
ENST00000218104.5:c.1555A>T ENSP00000218104.3:p.Ile519Phe
ENST00000443684.2:n.558A>T
NM_000033.3:c.1555A>T NP_000024.2:p.Ile519Phe
XR_938507.1:n.2027A>T
XR_938507.2:n.2027A>T
NM_000033.4:c.1555A>T MANE Select NP_000024.2:p.Ile519Phe
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