Canonical Allele Identifier: CA2690187550
Gene: FXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035694dup , CM000671.2:g.69035694dup GRCh38
NC_000009.11:g.71650610dup , CM000671.1:g.71650610dup GRCh37
NC_000009.10:g.70840430dup NCBI36
NG_008845.2:g.5132dup

Transcript Alleles

HGVS Amino-acid change
ENST00000377270.7:c.-89dup ENSP00000366482.3:n.-89dup
ENST00000396364.7:c.-89dup ENSP00000379650.3:n.-89dup
NM_000144.4:c.-89dup NP_000135.2:n.-89dup
NM_001161706.1:c.-89dup NP_001155178.1:n.-89dup
NM_181425.2:c.-89dup NP_852090.1:n.-89dup