Canonical Allele Identifier: CA193369020
Gene: FXN HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs140510894

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035886del , CM000671.2:g.69035886del GRCh38
NC_000009.11:g.71650802del , CM000671.1:g.71650802del GRCh37
NC_000009.10:g.70840622del NCBI36
NG_008845.2:g.5324del

Transcript Alleles

HGVS Amino-acid change
NM_000144.4:c.104del VV NP_000135.2:p.Pro35HisfsTer?
NM_001161706.1:c.104del VV NP_001155178.1:p.Pro35HisfsTer?
NM_181425.2:c.104del VV NP_852090.1:p.Pro35HisfsTer?
NM_000144.5:c.104del VV MANE Preferred
ENST00000377270.7:c.104del ENSP00000366482.3:p.Pro35HisfsTer?
ENST00000396364.7:c.104del ENSP00000379650.3:p.Pro35HisfsTer?
ENST00000396366.6:c.104del ENSP00000379652.2:p.Pro35HisfsTer?