Canonical Allele Identifier: CA373530994

Gene: FXN

Linked Data

• MyVariant Identifiers: chr9:g.71679955T>A (hg19) ; chr9:g.69065039T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69065039T>A , CM000671.2:g.69065039T>A	GRCh38
NC_000009.11:g.71679955T>A , CM000671.1:g.71679955T>A	GRCh37
NC_000009.10:g.70869775T>A	NCBI36
NG_008845.2:g.34477T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377270.8:c.257+4T>A	ENSP00000366482.4:n.257+4T>A
ENST00000484259.3:c.482+4T>A MANE Select	ENSP00000419243.2:n.482+4T>A
ENST00000642330.1:c.384+11779T>A	ENSP00000493770.1:n.384+11779T>A
ENST00000642889.1:c.165+29092T>A	ENSP00000493780.1:n.165+29092T>A
ENST00000643352.1:c.482+4T>A	ENSP00000496488.1:n.482+4T>A
ENST00000643765.1:c.480+4T>A
ENST00000644653.1:c.*85+4T>A	ENSP00000495217.1:n.*85+4T>A
ENST00000644977.1:c.*207+4T>A	ENSP00000495651.1:n.*207+4T>A
ENST00000645088.1:c.*85+4T>A	ENSP00000495447.1:n.*85+4T>A
ENST00000646862.1:c.384+11779T>A	ENSP00000494599.1:n.384+11779T>A
ENST00000377270.7:c.482+4T>A	ENSP00000366482.3:n.482+4T>A
ENST00000396364.7:c.482+4T>A	ENSP00000379650.3:n.482+4T>A
ENST00000396366.6:c.486T>A	ENSP00000379652.2:p.Tyr162Ter
ENST00000484259.1:c.174+4T>A
ENST00000498653.5:c.257+4T>A	ENSP00000418015.1:n.257+4T>A
NM_000144.4:c.482+4T>A	NP_000135.2:n.482+4T>A
NM_001161706.1:c.482+4T>A	NP_001155178.1:n.482+4T>A
NM_181425.2:c.486T>A	NP_852090.1:p.Tyr162Ter
NM_000144.5:c.482+4T>A MANE Select	NP_000135.2:n.482+4T>A
NM_181425.3:c.486T>A	NP_852090.1:p.Tyr162Ter