Canonical Allele Identifier: CA2579347335

Gene: FXN

Linked Data

• gnomAD v4: 9-69064927-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69064929del , CM000671.2:g.69064929del	GRCh38
NC_000009.11:g.71679845del , CM000671.1:g.71679845del	GRCh37
NC_000009.10:g.70869665del	NCBI36
NG_008845.2:g.34367del

Transcript Alleles

HGVS	Amino-acid change
ENST00000377270.8:c.160-9del	ENSP00000366482.4:n.160-9del
ENST00000484259.3:c.385-9del MANE Select	ENSP00000419243.2:n.385-9del
ENST00000642330.1:c.384+11669del	ENSP00000493770.1:n.384+11669del
ENST00000642889.1:c.165+28982del	ENSP00000493780.1:n.165+28982del
ENST00000643352.1:c.385-9del	ENSP00000496488.1:n.385-9del
ENST00000643765.1:c.383-9del
ENST00000644653.1:c.264-9del	ENSP00000495217.1:n.264-9del
ENST00000644977.1:c.*110-9del	ENSP00000495651.1:n.*110-9del
ENST00000645088.1:c.264-9del	ENSP00000495447.1:n.264-9del
ENST00000646862.1:c.384+11669del	ENSP00000494599.1:n.384+11669del
ENST00000377270.7:c.385-9del	ENSP00000366482.3:n.385-9del
ENST00000396364.7:c.385-9del	ENSP00000379650.3:n.385-9del
ENST00000396366.6:c.385-9del	ENSP00000379652.2:n.385-9del
ENST00000484259.1:c.77-9del
ENST00000498653.5:c.160-9del	ENSP00000418015.1:n.160-9del
NM_000144.4:c.385-9del	NP_000135.2:n.385-9del
NM_001161706.1:c.385-9del	NP_001155178.1:n.385-9del
NM_181425.2:c.385-9del	NP_852090.1:n.385-9del
NM_000144.5:c.385-9del MANE Select	NP_000135.2:n.385-9del
NM_181425.3:c.385-9del	NP_852090.1:n.385-9del