Canonical Allele Identifier: CA1854051732

Gene: FXN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69064856_69064857delinsTA , CM000671.2:g.69064856_69064857delinsTA	GRCh38
NC_000009.11:g.71679772_71679773delinsTA , CM000671.1:g.71679772_71679773delinsTA	GRCh37
NC_000009.10:g.70869592_70869593delinsTA	NCBI36
NG_008845.2:g.34294_34295delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000377270.8:c.160-82_160-81delinsTA	ENSP00000366482.4:n.160-82_160-81delinsTA...
ENST00000484259.3:c.385-82_385-81delinsTA MANE Select	ENSP00000419243.2:n.385-82_385-81delinsTA...
ENST00000642330.1:c.384+11596_384+11597delinsTA	ENSP00000493770.1:n.384+11596_384+11597de...
ENST00000642889.1:c.165+28909_165+28910delinsTA	ENSP00000493780.1:n.165+28909_165+28910de...
ENST00000643352.1:c.385-82_385-81delinsTA	ENSP00000496488.1:n.385-82_385-81delinsTA...
ENST00000643765.1:c.383-82_383-81delinsTA
ENST00000644653.1:c.264-82_264-81delinsTA	ENSP00000495217.1:n.264-82_264-81delinsTA...
ENST00000644977.1:c.*110-82_*110-81delinsTA	ENSP00000495651.1:n.*110-82_*110-81delins...
ENST00000645088.1:c.264-82_264-81delinsTA	ENSP00000495447.1:n.264-82_264-81delinsTA...
ENST00000646862.1:c.384+11596_384+11597delinsTA	ENSP00000494599.1:n.384+11596_384+11597de...
ENST00000377270.7:c.385-82_385-81delinsTA	ENSP00000366482.3:n.385-82_385-81delinsTA...
ENST00000396364.7:c.385-82_385-81delinsTA	ENSP00000379650.3:n.385-82_385-81delinsTA...
ENST00000396366.6:c.385-82_385-81delinsTA	ENSP00000379652.2:n.385-82_385-81delinsTA...
ENST00000484259.1:c.77-82_77-81delinsTA
ENST00000498653.5:c.160-82_160-81delinsTA	ENSP00000418015.1:n.160-82_160-81delinsTA...
NM_000144.4:c.385-82_385-81delinsTA	NP_000135.2:n.385-82_385-81delinsTA
NM_001161706.1:c.385-82_385-81delinsTA	NP_001155178.1:n.385-82_385-81delinsTA
NM_181425.2:c.385-82_385-81delinsTA	NP_852090.1:n.385-82_385-81delinsTA
NM_000144.5:c.385-82_385-81delinsTA MANE Select	NP_000135.2:n.385-82_385-81delinsTA
NM_181425.3:c.385-82_385-81delinsTA	NP_852090.1:n.385-82_385-81delinsTA