Canonical Allele Identifier: CA2690187648
Gene: FXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035772_69035877del , CM000671.2:g.69035772_69035877del GRCh38
NC_000009.11:g.71650688_71650793del , CM000671.1:g.71650688_71650793del GRCh37
NC_000009.10:g.70840508_70840613del NCBI36
NG_008845.2:g.5210_5315del

Transcript Alleles

HGVS Amino-acid change
ENST00000484259.3:c.-11_95del
ENST00000642330.1:c.-11_95del
ENST00000642889.1:c.-11_95del
ENST00000643352.1:c.-11_95del
ENST00000644653.1:c.-11_95del
ENST00000645088.1:c.-11_95del
ENST00000377270.7:c.-11_95del
ENST00000396364.7:c.-11_95del
ENST00000396366.6:c.-11_95del
NM_000144.4:c.-11_95del
NM_001161706.1:c.-11_95del
NM_181425.2:c.-11_95del
NM_000144.5:c.-11_95del
NM_181425.3:c.-11_95del