Canonical Allele Identifier: CA465233544
Gene: FXN HGNC NCBI

Linked Data

dbSNP Id: rs746185269

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69053254C>T , CM000671.2:g.69053254C>T GRCh38
NC_000009.11:g.71668170C>T , CM000671.1:g.71668170C>T GRCh37
NC_000009.10:g.70857990C>T NCBI36
NG_008845.2:g.22692C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377270.8:c.153C>T ENSP00000366482.4:p.Ser51=
ENST00000484259.3:c.378C>T MANE Select ENSP00000419243.2:p.Ser126=
ENST00000642330.1:c.378C>T ENSP00000493770.1:p.Ser126=
ENST00000642889.1:c.165+17307C>T ENSP00000493780.1:n.165+17307C>T
ENST00000643352.1:c.378C>T ENSP00000496488.1:p.Ser126=
ENST00000643765.1:c.376C>T
ENST00000644653.1:c.263+6772C>T ENSP00000495217.1:n.263+6772C>T
ENST00000644977.1:c.*103C>T ENSP00000495651.1:n.*103C>T
ENST00000645088.1:c.263+6772C>T ENSP00000495447.1:n.263+6772C>T
ENST00000646862.1:c.378C>T ENSP00000494599.1:p.Ser126=
ENST00000377270.7:c.378C>T ENSP00000366482.3:p.Ser126=
ENST00000396364.7:c.378C>T ENSP00000379650.3:p.Ser126=
ENST00000396366.6:c.378C>T ENSP00000379652.2:p.Ser126=
ENST00000484259.1:c.76+6772C>T
ENST00000498653.5:c.153C>T ENSP00000418015.1:p.Ser51=
NM_000144.4:c.378C>T NP_000135.2:p.Ser126=
NM_001161706.1:c.378C>T NP_001155178.1:p.Ser126=
NM_181425.2:c.378C>T NP_852090.1:p.Ser126=
NM_000144.5:c.378C>T MANE Select NP_000135.2:p.Ser126=
NM_181425.3:c.378C>T NP_852090.1:p.Ser126=