Canonical Allele Identifier: CA1854051802
Gene: FXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69064914_69064915delinsCT , CM000671.2:g.69064914_69064915delinsCT GRCh38
NC_000009.11:g.71679830_71679831delinsCT , CM000671.1:g.71679830_71679831delinsCT GRCh37
NC_000009.10:g.70869650_70869651delinsCT NCBI36
NG_008845.2:g.34352_34353delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000377270.8:c.160-24_160-23delinsCT ENSP00000366482.4:n.160-24_160-23delinsCT...
ENST00000484259.3:c.385-24_385-23delinsCT MANE Select ENSP00000419243.2:n.385-24_385-23delinsCT...
ENST00000642330.1:c.384+11654_384+11655delinsCT ENSP00000493770.1:n.384+11654_384+11655de...
ENST00000642889.1:c.165+28967_165+28968delinsCT ENSP00000493780.1:n.165+28967_165+28968de...
ENST00000643352.1:c.385-24_385-23delinsCT ENSP00000496488.1:n.385-24_385-23delinsCT...
ENST00000643765.1:c.383-24_383-23delinsCT
ENST00000644653.1:c.264-24_264-23delinsCT ENSP00000495217.1:n.264-24_264-23delinsCT...
ENST00000644977.1:c.*110-24_*110-23delinsCT ENSP00000495651.1:n.*110-24_*110-23delins...
ENST00000645088.1:c.264-24_264-23delinsCT ENSP00000495447.1:n.264-24_264-23delinsCT...
ENST00000646862.1:c.384+11654_384+11655delinsCT ENSP00000494599.1:n.384+11654_384+11655de...
ENST00000377270.7:c.385-24_385-23delinsCT ENSP00000366482.3:n.385-24_385-23delinsCT...
ENST00000396364.7:c.385-24_385-23delinsCT ENSP00000379650.3:n.385-24_385-23delinsCT...
ENST00000396366.6:c.385-24_385-23delinsCT ENSP00000379652.2:n.385-24_385-23delinsCT...
ENST00000484259.1:c.77-24_77-23delinsCT
ENST00000498653.5:c.160-24_160-23delinsCT ENSP00000418015.1:n.160-24_160-23delinsCT...
NM_000144.4:c.385-24_385-23delinsCT NP_000135.2:n.385-24_385-23delinsCT
NM_001161706.1:c.385-24_385-23delinsCT NP_001155178.1:n.385-24_385-23delinsCT
NM_181425.2:c.385-24_385-23delinsCT NP_852090.1:n.385-24_385-23delinsCT
NM_000144.5:c.385-24_385-23delinsCT MANE Select NP_000135.2:n.385-24_385-23delinsCT
NM_181425.3:c.385-24_385-23delinsCT NP_852090.1:n.385-24_385-23delinsCT