Canonical Allele Identifier: CA373530842
Gene: FXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69064989A>G , CM000671.2:g.69064989A>G GRCh38
NC_000009.11:g.71679905A>G , CM000671.1:g.71679905A>G GRCh37
NC_000009.10:g.70869725A>G NCBI36
NG_008845.2:g.34427A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377270.8:c.211A>G ENSP00000366482.4:p.Asn71Asp
ENST00000484259.3:c.436A>G MANE Select ENSP00000419243.2:p.Asn146Asp
ENST00000642330.1:c.384+11729A>G ENSP00000493770.1:n.384+11729A>G
ENST00000642889.1:c.165+29042A>G ENSP00000493780.1:n.165+29042A>G
ENST00000643352.1:c.436A>G ENSP00000496488.1:p.Asn146Asp
ENST00000643765.1:c.434A>G
ENST00000644653.1:c.*39A>G ENSP00000495217.1:n.*39A>G
ENST00000644977.1:c.*161A>G ENSP00000495651.1:n.*161A>G
ENST00000645088.1:c.*39A>G ENSP00000495447.1:n.*39A>G
ENST00000646862.1:c.384+11729A>G ENSP00000494599.1:n.384+11729A>G
ENST00000377270.7:c.436A>G ENSP00000366482.3:p.Asn146Asp
ENST00000396364.7:c.436A>G ENSP00000379650.3:p.Asn146Asp
ENST00000396366.6:c.436A>G ENSP00000379652.2:p.Asn146Asp
ENST00000484259.1:c.128A>G
ENST00000498653.5:c.211A>G ENSP00000418015.1:p.Asn71Asp
NM_000144.4:c.436A>G NP_000135.2:p.Asn146Asp
NM_001161706.1:c.436A>G NP_001155178.1:p.Asn146Asp
NM_181425.2:c.436A>G NP_852090.1:p.Asn146Asp
NM_000144.5:c.436A>G MANE Select NP_000135.2:p.Asn146Asp
NM_181425.3:c.436A>G NP_852090.1:p.Asn146Asp