Canonical Allele Identifier: CA1139767900
Gene: ABCD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153736098_153736099insA , CM000685.2:g.153736098_153736099insA GRCh38
NC_000023.10:g.153001552_153001553insA , CM000685.1:g.153001552_153001553insA GRCh37
NC_000023.9:g.152654746_152654747insA NCBI36
NG_009022.2:g.16231_16232insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000218104.6:c.1082-14_1082-13insA MANE Select ENSP00000218104.3:n.1082-14_1082-13insA
ENST00000218104.5:c.1082-14_1082-13insA ENSP00000218104.3:n.1082-14_1082-13insA
ENST00000443684.2:n.85-14_85-13insA
NM_000033.3:c.1082-14_1082-13insA NP_000024.2:n.1082-14_1082-13insA
XR_938507.1:n.1498-14_1498-13insA
XR_938507.2:n.1498-14_1498-13insA
NM_000033.4:c.1082-14_1082-13insA MANE Select NP_000024.2:n.1082-14_1082-13insA