Canonical Allele Identifier: CA465233583

Gene: FXN

Linked Data

• MyVariant Identifiers: chr9:g.71679886T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69064970T>C , CM000671.2:g.69064970T>C	GRCh38
NC_000009.11:g.71679886T>C , CM000671.1:g.71679886T>C	GRCh37
NC_000009.10:g.70869706T>C	NCBI36
NG_008845.2:g.34408T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377270.8:c.192T>C	ENSP00000366482.4:p.Asp64=
ENST00000484259.3:c.417T>C MANE Select	ENSP00000419243.2:p.Asp139=
ENST00000642330.1:c.384+11710T>C	ENSP00000493770.1:n.384+11710T>C
ENST00000642889.1:c.165+29023T>C	ENSP00000493780.1:n.165+29023T>C
ENST00000643352.1:c.417T>C	ENSP00000496488.1:p.Asp139=
ENST00000643765.1:c.415T>C
ENST00000644653.1:c.*20T>C	ENSP00000495217.1:n.*20T>C
ENST00000644977.1:c.*142T>C	ENSP00000495651.1:n.*142T>C
ENST00000645088.1:c.*20T>C	ENSP00000495447.1:n.*20T>C
ENST00000646862.1:c.384+11710T>C	ENSP00000494599.1:n.384+11710T>C
ENST00000377270.7:c.417T>C	ENSP00000366482.3:p.Asp139=
ENST00000396364.7:c.417T>C	ENSP00000379650.3:p.Asp139=
ENST00000396366.6:c.417T>C	ENSP00000379652.2:p.Asp139=
ENST00000484259.1:c.109T>C
ENST00000498653.5:c.192T>C	ENSP00000418015.1:p.Asp64=
NM_000144.4:c.417T>C	NP_000135.2:p.Asp139=
NM_001161706.1:c.417T>C	NP_001155178.1:p.Asp139=
NM_181425.2:c.417T>C	NP_852090.1:p.Asp139=
NM_000144.5:c.417T>C MANE Select	NP_000135.2:p.Asp139=
NM_181425.3:c.417T>C	NP_852090.1:p.Asp139=