Canonical Allele Identifier: CA2466456781
Gene: ABCD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153741110T= , CM000685.2:g.153741110T= GRCh38
NC_000023.10:g.153006564T= , CM000685.1:g.153006564T= GRCh37
NC_000023.9:g.152659758T= NCBI36
NG_009022.2:g.21243T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1780+391T= MANE Select ENSP00000218104.3:n.1780+391T=
ENST00000218104.5:c.1780+391T= ENSP00000218104.3:n.1780+391T=
NM_000033.3:c.1780+391T= NP_000024.2:n.1780+391T=
XR_938507.1:n.2252+391T=
XR_938507.2:n.2252+391T=
NM_000033.4:c.1780+391T= MANE Select NP_000024.2:n.1780+391T=