Canonical Allele Identifier: CA373527301

Gene: FXN

Linked Data

• MyVariant Identifiers: chr9:g.71650735C>A (hg19) ; chr9:g.69035819C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69035819C>A , CM000671.2:g.69035819C>A	GRCh38
NC_000009.11:g.71650735C>A , CM000671.1:g.71650735C>A	GRCh37
NC_000009.10:g.70840555C>A	NCBI36
NG_008845.2:g.5257C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000484259.3:c.37C>A MANE Select	ENSP00000419243.2:p.Leu13Met
ENST00000642330.1:c.37C>A	ENSP00000493770.1:p.Leu13Met
ENST00000642889.1:c.37C>A	ENSP00000493780.1:p.Leu13Met
ENST00000643352.1:c.37C>A	ENSP00000496488.1:p.Leu13Met
ENST00000643765.1:c.35C>A
ENST00000644653.1:c.37C>A	ENSP00000495217.1:p.Leu13Met
ENST00000644977.1:c.37C>A	ENSP00000495651.1:p.Leu13Met
ENST00000645088.1:c.37C>A	ENSP00000495447.1:p.Leu13Met
ENST00000646862.1:c.37C>A	ENSP00000494599.1:p.Leu13Met
ENST00000377270.7:c.37C>A	ENSP00000366482.3:p.Leu13Met
ENST00000396364.7:c.37C>A	ENSP00000379650.3:p.Leu13Met
ENST00000396366.6:c.37C>A	ENSP00000379652.2:p.Leu13Met
NM_000144.4:c.37C>A	NP_000135.2:p.Leu13Met
NM_001161706.1:c.37C>A	NP_001155178.1:p.Leu13Met
NM_181425.2:c.37C>A	NP_852090.1:p.Leu13Met
NM_000144.5:c.37C>A MANE Select	NP_000135.2:p.Leu13Met
NM_181425.3:c.37C>A	NP_852090.1:p.Leu13Met