Canonical Allele Identifier: CA1854051663

Gene: FXN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69064783_69064785delinsCCT , CM000671.2:g.69064783_69064785delinsCCT	GRCh38
NC_000009.11:g.71679699_71679701delinsCCT , CM000671.1:g.71679699_71679701delinsCCT	GRCh37
NC_000009.10:g.70869519_70869521delinsCCT	NCBI36
NG_008845.2:g.34221_34223delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377270.8:c.160-155_160-153delinsCCT	ENSP00000366482.4:n.160-155_160-153delinsCCT
ENST00000484259.3:c.385-155_385-153delinsCCT MANE Select	ENSP00000419243.2:n.385-155_385-153delinsCCT
ENST00000642330.1:c.384+11523_384+11525delinsCCT	ENSP00000493770.1:n.384+11523_384+11525delinsCCT
ENST00000642889.1:c.165+28836_165+28838delinsCCT	ENSP00000493780.1:n.165+28836_165+28838delinsCCT
ENST00000643352.1:c.385-155_385-153delinsCCT	ENSP00000496488.1:n.385-155_385-153delinsCCT
ENST00000643765.1:c.383-155_383-153delinsCCT
ENST00000644653.1:c.264-155_264-153delinsCCT	ENSP00000495217.1:n.264-155_264-153delinsCCT
ENST00000644977.1:c.*110-155_*110-153delinsCCT	ENSP00000495651.1:n.*110-155_*110-153delinsCCT
ENST00000645088.1:c.264-155_264-153delinsCCT	ENSP00000495447.1:n.264-155_264-153delinsCCT
ENST00000646862.1:c.384+11523_384+11525delinsCCT	ENSP00000494599.1:n.384+11523_384+11525delinsCCT
ENST00000377270.7:c.385-155_385-153delinsCCT	ENSP00000366482.3:n.385-155_385-153delinsCCT
ENST00000396364.7:c.385-155_385-153delinsCCT	ENSP00000379650.3:n.385-155_385-153delinsCCT
ENST00000396366.6:c.385-155_385-153delinsCCT	ENSP00000379652.2:n.385-155_385-153delinsCCT
ENST00000484259.1:c.77-155_77-153delinsCCT
ENST00000498653.5:c.160-155_160-153delinsCCT	ENSP00000418015.1:n.160-155_160-153delinsCCT
NM_000144.4:c.385-155_385-153delinsCCT	NP_000135.2:n.385-155_385-153delinsCCT
NM_001161706.1:c.385-155_385-153delinsCCT	NP_001155178.1:n.385-155_385-153delinsCCT
NM_181425.2:c.385-155_385-153delinsCCT	NP_852090.1:n.385-155_385-153delinsCCT
NM_000144.5:c.385-155_385-153delinsCCT MANE Select	NP_000135.2:n.385-155_385-153delinsCCT
NM_181425.3:c.385-155_385-153delinsCCT	NP_852090.1:n.385-155_385-153delinsCCT