Canonical Allele Identifier: CA1854051882

Gene: FXN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69064968G= , CM000671.2:g.69064968G=	GRCh38
NC_000009.11:g.71679884G= , CM000671.1:g.71679884G=	GRCh37
NC_000009.10:g.70869704G=	NCBI36
NG_008845.2:g.34406G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377270.8:c.190G=	ENSP00000366482.4:p.Asp64=
ENST00000484259.3:c.415G= MANE Select	ENSP00000419243.2:p.Asp139=
ENST00000642330.1:c.384+11708G=	ENSP00000493770.1:n.384+11708G=
ENST00000642889.1:c.165+29021G=	ENSP00000493780.1:n.165+29021G=
ENST00000643352.1:c.415G=	ENSP00000496488.1:p.Asp139=
ENST00000643765.1:c.413G=
ENST00000644653.1:c.*18G=	ENSP00000495217.1:n.*18G=
ENST00000644977.1:c.*140G=	ENSP00000495651.1:n.*140G=
ENST00000645088.1:c.*18G=	ENSP00000495447.1:n.*18G=
ENST00000646862.1:c.384+11708G=	ENSP00000494599.1:n.384+11708G=
ENST00000377270.7:c.415G=	ENSP00000366482.3:p.Asp139=
ENST00000396364.7:c.415G=	ENSP00000379650.3:p.Asp139=
ENST00000396366.6:c.415G=	ENSP00000379652.2:p.Asp139=
ENST00000484259.1:c.107G=
ENST00000498653.5:c.190G=	ENSP00000418015.1:p.Asp64=
NM_000144.4:c.415G=	NP_000135.2:p.Asp139=
NM_001161706.1:c.415G=	NP_001155178.1:p.Asp139=
NM_181425.2:c.415G=	NP_852090.1:p.Asp139=
NM_000144.5:c.415G= MANE Select	NP_000135.2:p.Asp139=
NM_181425.3:c.415G=	NP_852090.1:p.Asp139=