Canonical Allele Identifier: CA2466456446
Gene: ABCD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153740201A= , CM000685.2:g.153740201A= GRCh38
NC_000023.10:g.153005655A= , CM000685.1:g.153005655A= GRCh37
NC_000023.9:g.152658849A= NCBI36
NG_009022.2:g.20334A=

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.1598A= MANE Select ENSP00000218104.3:p.Lys533=
ENST00000218104.5:c.1598A= ENSP00000218104.3:p.Lys533=
ENST00000443684.2:n.601A=
NM_000033.3:c.1598A= NP_000024.2:p.Lys533=
XR_938507.1:n.2070A=
XR_938507.2:n.2070A=
NM_000033.4:c.1598A= MANE Select NP_000024.2:p.Lys533=