Canonical Allele Identifier: CA2466456442
Gene: ABCD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153740189G= , CM000685.2:g.153740189G= GRCh38
NC_000023.10:g.153005643G= , CM000685.1:g.153005643G= GRCh37
NC_000023.9:g.152658837G= NCBI36
NG_009022.2:g.20322G=

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1586G= MANE Select ENSP00000218104.3:p.Gly529=
ENST00000218104.5:c.1586G= ENSP00000218104.3:p.Gly529=
ENST00000443684.2:n.589G=
NM_000033.3:c.1586G= NP_000024.2:p.Gly529=
XR_938507.1:n.2058G=
XR_938507.2:n.2058G=
NM_000033.4:c.1586G= MANE Select NP_000024.2:p.Gly529=