Canonical Allele Identifier: CA373530776
Gene: FXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69064956A>T , CM000671.2:g.69064956A>T GRCh38
NC_000009.11:g.71679872A>T , CM000671.1:g.71679872A>T GRCh37
NC_000009.10:g.70869692A>T NCBI36
NG_008845.2:g.34394A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377270.8:c.178A>T ENSP00000366482.4:p.Lys60Ter
ENST00000484259.3:c.403A>T MANE Select ENSP00000419243.2:p.Lys135Ter
ENST00000642330.1:c.384+11696A>T ENSP00000493770.1:n.384+11696A>T
ENST00000642889.1:c.165+29009A>T ENSP00000493780.1:n.165+29009A>T
ENST00000643352.1:c.403A>T ENSP00000496488.1:p.Lys135Ter
ENST00000643765.1:c.401A>T
ENST00000644653.1:c.*6A>T ENSP00000495217.1:n.*6A>T
ENST00000644977.1:c.*128A>T ENSP00000495651.1:n.*128A>T
ENST00000645088.1:c.*6A>T ENSP00000495447.1:n.*6A>T
ENST00000646862.1:c.384+11696A>T ENSP00000494599.1:n.384+11696A>T
ENST00000377270.7:c.403A>T ENSP00000366482.3:p.Lys135Ter
ENST00000396364.7:c.403A>T ENSP00000379650.3:p.Lys135Ter
ENST00000396366.6:c.403A>T ENSP00000379652.2:p.Lys135Ter
ENST00000484259.1:c.95A>T
ENST00000498653.5:c.178A>T ENSP00000418015.1:p.Lys60Ter
NM_000144.4:c.403A>T NP_000135.2:p.Lys135Ter
NM_001161706.1:c.403A>T NP_001155178.1:p.Lys135Ter
NM_181425.2:c.403A>T NP_852090.1:p.Lys135Ter
NM_000144.5:c.403A>T MANE Select NP_000135.2:p.Lys135Ter
NM_181425.3:c.403A>T NP_852090.1:p.Lys135Ter