Canonical Allele Identifier: CA1854065142

Gene: FXN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69072646T= , CM000671.2:g.69072646T=	GRCh38
NC_000009.11:g.71687562T= , CM000671.1:g.71687562T=	GRCh37
NC_000009.10:g.70877382T=	NCBI36
NG_008845.2:g.42084T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000144.5:c.517T= MANE Select	NP_000135.2:p.Trp173=
ENST00000484259.3:c.517T= MANE Select	ENSP00000419243.2:p.Trp173=
NM_000144.4:c.517T=	NP_000135.2:p.Trp173=
NM_001161706.1:c.482+7611T=	NP_001155178.1:n.482+7611T=
NM_181425.2:c.525T=	NP_852090.1:p.Thr175=
NM_181425.3:c.525T=	NP_852090.1:p.Thr175=
ENST00000377270.7:c.517T=	ENSP00000366482.3:p.Trp173=
ENST00000377270.8:c.292T=	ENSP00000366482.4:p.Trp98=
ENST00000396364.7:c.482+7611T=	ENSP00000379650.3:n.482+7611T=
ENST00000396366.6:c.525T=	ENSP00000379652.2:p.Thr175=
ENST00000484259.1:c.209T=
ENST00000498653.5:c.292T=	ENSP00000418015.1:p.Trp98=
ENST00000642330.1:c.384+19386T=	ENSP00000493770.1:n.384+19386T=
ENST00000642889.1:c.166-27255T=	ENSP00000493780.1:n.166-27255T=
ENST00000643352.1:c.482+7611T=	ENSP00000496488.1:n.482+7611T=
ENST00000643765.1:c.480+7611T=
ENST00000644653.1:c.*120T=	ENSP00000495217.1:n.*120T=
ENST00000644977.1:c.*207+7611T=	ENSP00000495651.1:n.*207+7611T=
ENST00000645088.1:c.*85+7611T=	ENSP00000495447.1:n.*85+7611T=
ENST00000646862.1:c.384+19386T=	ENSP00000494599.1:n.384+19386T=