Canonical Allele Identifier: CA1854065044
Gene: FXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69072611G= , CM000671.2:g.69072611G= GRCh38
NC_000009.11:g.71687527G= , CM000671.1:g.71687527G= GRCh37
NC_000009.10:g.70877347G= NCBI36
NG_008845.2:g.42049G=

Transcript Alleles

HGVS Amino-acid change
ENST00000377270.8:c.258-1G= ENSP00000366482.4:n.258-1G=
ENST00000484259.3:c.483-1G= MANE Select ENSP00000419243.2:n.483-1G=
ENST00000642330.1:c.384+19351G= ENSP00000493770.1:n.384+19351G=
ENST00000642889.1:c.166-27290G= ENSP00000493780.1:n.166-27290G=
ENST00000643352.1:c.482+7576G= ENSP00000496488.1:n.482+7576G=
ENST00000643765.1:c.480+7576G=
ENST00000644653.1:c.*86-1G= ENSP00000495217.1:n.*86-1G=
ENST00000644977.1:c.*207+7576G= ENSP00000495651.1:n.*207+7576G=
ENST00000645088.1:c.*85+7576G= ENSP00000495447.1:n.*85+7576G=
ENST00000646862.1:c.384+19351G= ENSP00000494599.1:n.384+19351G=
ENST00000377270.7:c.483-1G= ENSP00000366482.3:n.483-1G=
ENST00000396364.7:c.482+7576G= ENSP00000379650.3:n.482+7576G=
ENST00000396366.6:c.491-1G= ENSP00000379652.2:n.491-1G=
ENST00000484259.1:c.175-1G=
ENST00000498653.5:c.258-1G= ENSP00000418015.1:n.258-1G=
NM_000144.4:c.483-1G= NP_000135.2:n.483-1G=
NM_001161706.1:c.482+7576G= NP_001155178.1:n.482+7576G=
NM_181425.2:c.491-1G= NP_852090.1:n.491-1G=
NM_000144.5:c.483-1G= MANE Select NP_000135.2:n.483-1G=
NM_181425.3:c.491-1G= NP_852090.1:n.491-1G=