Canonical Allele Identifier: CA588647896

Gene: FXN

Linked Data

• dbSNP Id: rs145006100
• gnomAD v2: 9-71650692-G-C
• gnomAD v4: 9-69035776-G-C
• MyVariant Identifiers: chr9:g.71650692G>C (hg19) ; chr9:g.69035776G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69035776G>C , CM000671.2:g.69035776G>C	GRCh38
NC_000009.11:g.71650692G>C , CM000671.1:g.71650692G>C	GRCh37
NC_000009.10:g.70840512G>C	NCBI36
NG_008845.2:g.5214G>C

Transcript Alleles

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