Canonical Allele Identifier: CA373623601

Gene: FXN

Linked Data

• MyVariant Identifiers: chr9:g.71687577G>C (hg19) ; chr9:g.69072661G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69072661G>C , CM000671.2:g.69072661G>C	GRCh38
NC_000009.11:g.71687577G>C , CM000671.1:g.71687577G>C	GRCh37
NC_000009.10:g.70877397G>C	NCBI36
NG_008845.2:g.42099G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377270.8:c.307G>C	ENSP00000366482.4:p.Asp103His
ENST00000484259.3:c.532G>C MANE Select	ENSP00000419243.2:p.Asp178His
ENST00000642330.1:c.384+19401G>C	ENSP00000493770.1:n.384+19401G>C
ENST00000642889.1:c.166-27240G>C	ENSP00000493780.1:n.166-27240G>C
ENST00000643352.1:c.482+7626G>C	ENSP00000496488.1:n.482+7626G>C
ENST00000643765.1:c.480+7626G>C
ENST00000644653.1:c.*135G>C	ENSP00000495217.1:n.*135G>C
ENST00000644977.1:c.*207+7626G>C	ENSP00000495651.1:n.*207+7626G>C
ENST00000645088.1:c.*85+7626G>C	ENSP00000495447.1:n.*85+7626G>C
ENST00000646862.1:c.384+19401G>C	ENSP00000494599.1:n.384+19401G>C
ENST00000377270.7:c.532G>C	ENSP00000366482.3:p.Asp178His
ENST00000396364.7:c.482+7626G>C	ENSP00000379650.3:n.482+7626G>C
ENST00000396366.6:c.540G>C	ENSP00000379652.2:p.Thr180=
ENST00000484259.1:c.224G>C
ENST00000498653.5:c.307G>C	ENSP00000418015.1:p.Asp103His
NM_000144.4:c.532G>C	NP_000135.2:p.Asp178His
NM_001161706.1:c.482+7626G>C	NP_001155178.1:n.482+7626G>C
NM_181425.2:c.540G>C	NP_852090.1:p.Thr180=
NM_000144.5:c.532G>C MANE Select	NP_000135.2:p.Asp178His
NM_181425.3:c.540G>C	NP_852090.1:p.Thr180=