Canonical Allele Identifier: CA1978639247
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220642T= , CM000673.2:g.64220642T= GRCh38
NC_000011.9:g.63988114T= , CM000673.1:g.63988114T= GRCh37
NC_000011.8:g.63744690T= NCBI36
NG_016360.1:g.18963T= , LRG_180:g.18963T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1530T= ENSP00000279227.5:p.Arg510=
ENST00000540554.2:n.2696T=
ENST00000541252.2:c.978T= ENSP00000438885.2:p.Arg326=
ENST00000541326.6:n.939T=
ENST00000544997.6:c.1518T= ENSP00000445778.2:p.Arg506=
ENST00000545896.2:c.207T= ENSP00000440209.2:p.Arg69=
ENST00000546255.2:n.1822T=
ENST00000698845.1:c.*713T= ENSP00000513981.1:n.*713T=
ENST00000698846.1:n.1764T=
ENST00000698847.1:c.*923T= ENSP00000513982.1:n.*923T=
ENST00000698849.1:n.638T=
ENST00000698850.1:n.1286T=
ENST00000698852.1:c.1518T= ENSP00000513984.1:p.Arg506=
ENST00000698853.1:c.*747T= ENSP00000513985.1:n.*747T=
ENST00000698854.1:c.*848T= ENSP00000513986.1:n.*848T=
ENST00000698855.1:n.3170T=
ENST00000698856.1:n.2864T=
ENST00000698859.1:n.1682T=
ENST00000698860.1:c.1530T= ENSP00000513988.1:p.Arg510=
ENST00000698861.1:c.1518T= ENSP00000513989.1:p.Arg506=
ENST00000698862.1:c.*814T= ENSP00000513990.1:n.*814T=
ENST00000698863.1:c.1518T= ENSP00000513991.1:p.Arg506=
ENST00000698864.1:n.1733T=
ENST00000698865.1:c.1539T= ENSP00000513992.1:p.Arg513=
ENST00000698866.1:c.*1032T= ENSP00000513993.1:n.*1032T=
ENST00000698867.1:n.5493T=
ENST00000698868.1:c.1383T= ENSP00000513994.1:p.Arg461=
ENST00000698869.1:c.1311+316T= ENSP00000513995.1:n.1311+316T=
ENST00000698870.1:c.1518T= ENSP00000513996.1:p.Arg506=
ENST00000698871.1:n.2041T=
ENST00000698872.1:c.*307T= ENSP00000513997.1:n.*307T=
ENST00000698873.1:c.*713T= ENSP00000513998.1:n.*713T=
ENST00000698874.1:c.978T= ENSP00000513999.1:p.Arg326=
ENST00000698875.1:n.1378T=
ENST00000698876.1:n.1566T=
ENST00000698877.1:n.1086T=
ENST00000698878.1:c.1512T= ENSP00000514000.1:p.Arg504=
ENST00000698880.1:c.1386T=
ENST00000345728.10:c.1518T= MANE Select ENSP00000339950.5:p.Arg506=
ENST00000279227.9:c.1530T= ENSP00000279227.5:p.Arg510=
ENST00000345728.9:c.1518T= ENSP00000339950.5:p.Arg506=
ENST00000545896.1:c.206T= ENSP00000440209.1:p.Val69=
NM_031471.5:c.1518T= NP_113659.3:p.Arg506=
NM_178443.2:c.1530T= , LRG_180t1:c.1530T= NP_848537.1:p.Arg510=
XM_011545294.1:c.1530T= XP_011543596.1:p.Arg510=
XM_011545295.1:c.990T= XP_011543597.1:p.Arg330=
XM_011545296.1:c.990T= XP_011543598.1:p.Arg330=
XM_011545294.3:c.1530T= XP_011543596.1:p.Arg510=
XM_011545295.2:c.990T= XP_011543597.1:p.Arg330=
XM_017018398.2:c.1518T= XP_016873887.1:p.Arg506=
XM_017018399.1:c.978T= XP_016873888.1:p.Arg326=
NM_031471.6:c.1518T= MANE Select NP_113659.3:p.Arg506=
NM_001382361.1:c.1518T= NP_001369290.1:p.Arg506=
NM_001382362.1:c.1530T= NP_001369291.1:p.Arg510=
NM_001382363.1:c.978T= NP_001369292.1:p.Arg326=
NM_001382364.1:c.990T= NP_001369293.1:p.Arg330=
NM_001382448.1:c.1518T= NP_001369377.1:p.Arg506=
NM_178443.3:c.1530T= NP_848537.1:p.Arg510=