Canonical Allele Identifier: CA2690187559
Gene: FXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035699_69035705del , CM000671.2:g.69035699_69035705del GRCh38
NC_000009.11:g.71650615_71650621del , CM000671.1:g.71650615_71650621del GRCh37
NC_000009.10:g.70840435_70840441del NCBI36
NG_008845.2:g.5137_5143del

Transcript Alleles

HGVS Amino-acid Change
ENST00000377270.7:c.-84_-78del ENSP00000366482.3:n.-84_-78del
ENST00000396364.7:c.-84_-78del ENSP00000379650.3:n.-84_-78del
NM_000144.4:c.-84_-78del NP_000135.2:n.-84_-78del
NM_001161706.1:c.-84_-78del NP_001155178.1:n.-84_-78del
NM_181425.2:c.-84_-78del NP_852090.1:n.-84_-78del