Canonical Allele Identifier: CA373530760
Gene: FXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69064948T>G , CM000671.2:g.69064948T>G GRCh38
NC_000009.11:g.71679864T>G , CM000671.1:g.71679864T>G GRCh37
NC_000009.10:g.70869684T>G NCBI36
NG_008845.2:g.34386T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000377270.8:c.170T>G ENSP00000366482.4:p.Leu57Ter
ENST00000484259.3:c.395T>G MANE Select ENSP00000419243.2:p.Leu132Ter
ENST00000642330.1:c.384+11688T>G ENSP00000493770.1:n.384+11688T>G
ENST00000642889.1:c.165+29001T>G ENSP00000493780.1:n.165+29001T>G
ENST00000643352.1:c.395T>G ENSP00000496488.1:p.Leu132Ter
ENST00000643765.1:c.393T>G
ENST00000644653.1:c.274T>G ENSP00000495217.1:p.Ter92Glu
ENST00000644977.1:c.*120T>G ENSP00000495651.1:n.*120T>G
ENST00000645088.1:c.274T>G ENSP00000495447.1:p.Ter92Glu
ENST00000646862.1:c.384+11688T>G ENSP00000494599.1:n.384+11688T>G
ENST00000377270.7:c.395T>G ENSP00000366482.3:p.Leu132Ter
ENST00000396364.7:c.395T>G ENSP00000379650.3:p.Leu132Ter
ENST00000396366.6:c.395T>G ENSP00000379652.2:p.Leu132Ter
ENST00000484259.1:c.87T>G
ENST00000498653.5:c.170T>G ENSP00000418015.1:p.Leu57Ter
NM_000144.4:c.395T>G NP_000135.2:p.Leu132Ter
NM_001161706.1:c.395T>G NP_001155178.1:p.Leu132Ter
NM_181425.2:c.395T>G NP_852090.1:p.Leu132Ter
NM_000144.5:c.395T>G MANE Select NP_000135.2:p.Leu132Ter
NM_181425.3:c.395T>G NP_852090.1:p.Leu132Ter