Canonical Allele Identifier: CA1854052004

Gene: FXN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69065037T= , CM000671.2:g.69065037T=	GRCh38
NC_000009.11:g.71679953T= , CM000671.1:g.71679953T=	GRCh37
NC_000009.10:g.70869773T=	NCBI36
NG_008845.2:g.34475T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377270.8:c.257+2T=	ENSP00000366482.4:n.257+2T=
ENST00000484259.3:c.482+2T= MANE Select	ENSP00000419243.2:n.482+2T=
ENST00000642330.1:c.384+11777T=	ENSP00000493770.1:n.384+11777T=
ENST00000642889.1:c.165+29090T=	ENSP00000493780.1:n.165+29090T=
ENST00000643352.1:c.482+2T=	ENSP00000496488.1:n.482+2T=
ENST00000643765.1:c.480+2T=
ENST00000644653.1:c.*85+2T=	ENSP00000495217.1:n.*85+2T=
ENST00000644977.1:c.*207+2T=	ENSP00000495651.1:n.*207+2T=
ENST00000645088.1:c.*85+2T=	ENSP00000495447.1:n.*85+2T=
ENST00000646862.1:c.384+11777T=	ENSP00000494599.1:n.384+11777T=
ENST00000377270.7:c.482+2T=	ENSP00000366482.3:n.482+2T=
ENST00000396364.7:c.482+2T=	ENSP00000379650.3:n.482+2T=
ENST00000396366.6:c.484T=	ENSP00000379652.2:p.Tyr162=
ENST00000484259.1:c.174+2T=
ENST00000498653.5:c.257+2T=	ENSP00000418015.1:n.257+2T=
NM_000144.4:c.482+2T=	NP_000135.2:n.482+2T=
NM_001161706.1:c.482+2T=	NP_001155178.1:n.482+2T=
NM_181425.2:c.484T=	NP_852090.1:p.Tyr162=
NM_000144.5:c.482+2T= MANE Select	NP_000135.2:n.482+2T=
NM_181425.3:c.484T=	NP_852090.1:p.Tyr162=