Canonical Allele Identifier: CA2690187659

Gene: FXN

Linked Data

• gnomAD v4: 9-69035774-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69035774C>A , CM000671.2:g.69035774C>A	GRCh38
NC_000009.11:g.71650690C>A , CM000671.1:g.71650690C>A	GRCh37
NC_000009.10:g.70840510C>A	NCBI36
NG_008845.2:g.5212C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484259.3:c.-9C>A MANE Select	ENSP00000419243.2:n.-9C>A
ENST00000642330.1:c.-9C>A	ENSP00000493770.1:n.-9C>A
ENST00000642889.1:c.-9C>A	ENSP00000493780.1:n.-9C>A
ENST00000643352.1:c.-9C>A	ENSP00000496488.1:n.-9C>A
ENST00000644653.1:c.-9C>A	ENSP00000495217.1:n.-9C>A
ENST00000645088.1:c.-9C>A	ENSP00000495447.1:n.-9C>A
ENST00000646862.1:c.-9C>A	ENSP00000494599.1:n.-9C>A
ENST00000377270.7:c.-9C>A	ENSP00000366482.3:n.-9C>A
ENST00000396364.7:c.-9C>A	ENSP00000379650.3:n.-9C>A
ENST00000396366.6:c.-9C>A	ENSP00000379652.2:n.-9C>A
NM_000144.4:c.-9C>A	NP_000135.2:n.-9C>A
NM_001161706.1:c.-9C>A	NP_001155178.1:n.-9C>A
NM_181425.2:c.-9C>A	NP_852090.1:n.-9C>A
NM_000144.5:c.-9C>A MANE Select	NP_000135.2:n.-9C>A
NM_181425.3:c.-9C>A	NP_852090.1:n.-9C>A