Canonical Allele Identifier: CA373623613

Gene: FXN

Linked Data

• MyVariant Identifiers: chr9:g.71687581G>A (hg19) ; chr9:g.69072665G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69072665G>A , CM000671.2:g.69072665G>A	GRCh38
NC_000009.11:g.71687581G>A , CM000671.1:g.71687581G>A	GRCh37
NC_000009.10:g.70877401G>A	NCBI36
NG_008845.2:g.42103G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377270.8:c.311G>A	ENSP00000366482.4:p.Gly104Asp
ENST00000484259.3:c.536G>A MANE Select	ENSP00000419243.2:p.Gly179Asp
ENST00000642330.1:c.384+19405G>A	ENSP00000493770.1:n.384+19405G>A
ENST00000642889.1:c.166-27236G>A	ENSP00000493780.1:n.166-27236G>A
ENST00000643352.1:c.482+7630G>A	ENSP00000496488.1:n.482+7630G>A
ENST00000643765.1:c.480+7630G>A
ENST00000644653.1:c.*139G>A	ENSP00000495217.1:n.*139G>A
ENST00000644977.1:c.*207+7630G>A	ENSP00000495651.1:n.*207+7630G>A
ENST00000645088.1:c.*85+7630G>A	ENSP00000495447.1:n.*85+7630G>A
ENST00000646862.1:c.384+19405G>A	ENSP00000494599.1:n.384+19405G>A
ENST00000377270.7:c.536G>A	ENSP00000366482.3:p.Gly179Asp
ENST00000396364.7:c.482+7630G>A	ENSP00000379650.3:n.482+7630G>A
ENST00000396366.6:c.544G>A	ENSP00000379652.2:p.Ala182Thr
ENST00000484259.1:c.228G>A
ENST00000498653.5:c.311G>A	ENSP00000418015.1:p.Gly104Asp
NM_000144.4:c.536G>A	NP_000135.2:p.Gly179Asp
NM_001161706.1:c.482+7630G>A	NP_001155178.1:n.482+7630G>A
NM_181425.2:c.544G>A	NP_852090.1:p.Ala182Thr
NM_000144.5:c.536G>A MANE Select	NP_000135.2:p.Gly179Asp
NM_181425.3:c.544G>A	NP_852090.1:p.Ala182Thr