Canonical Allele Identifier: CA475151849
Gene: FERMT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220640dup , CM000673.2:g.64220640dup GRCh38
NC_000011.9:g.63988112dup , CM000673.1:g.63988112dup GRCh37
NC_000011.8:g.63744688dup NCBI36
NG_016360.1:g.18961dup , LRG_180:g.18961dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1528dup ENSP00000279227.5:p.Arg510ProfsTer?
ENST00000540554.2:n.2694dup
ENST00000541252.2:c.976dup ENSP00000438885.2:p.Arg326ProfsTer?
ENST00000541326.6:n.937dup
ENST00000544997.6:c.1516dup ENSP00000445778.2:p.Arg506ProfsTer?
ENST00000545896.2:c.205dup ENSP00000440209.2:p.Arg69ProfsTer28
ENST00000546255.2:n.1820dup
ENST00000698845.1:c.*711dup ENSP00000513981.1:n.*711dup
ENST00000698846.1:n.1762dup
ENST00000698847.1:c.*921dup ENSP00000513982.1:n.*921dup
ENST00000698849.1:n.636dup
ENST00000698850.1:n.1284dup
ENST00000698852.1:c.1516dup ENSP00000513984.1:p.Arg506ProfsTer?
ENST00000698853.1:c.*745dup ENSP00000513985.1:n.*745dup
ENST00000698854.1:c.*846dup ENSP00000513986.1:n.*846dup
ENST00000698855.1:n.3168dup
ENST00000698856.1:n.2862dup
ENST00000698859.1:n.1680dup
ENST00000698860.1:c.1528dup ENSP00000513988.1:p.Arg510ProfsTer?
ENST00000698861.1:c.1516dup ENSP00000513989.1:p.Arg506ProfsTer?
ENST00000698862.1:c.*812dup ENSP00000513990.1:n.*812dup
ENST00000698863.1:c.1516dup ENSP00000513991.1:p.Arg506ProfsTer?
ENST00000698864.1:n.1731dup
ENST00000698865.1:c.1537dup ENSP00000513992.1:p.Arg513ProfsTer?
ENST00000698866.1:c.*1030dup ENSP00000513993.1:n.*1030dup
ENST00000698867.1:n.5491dup
ENST00000698868.1:c.1381dup ENSP00000513994.1:p.Arg461ProfsTer?
ENST00000698869.1:c.1311+314dup ENSP00000513995.1:n.1311+314dup
ENST00000698870.1:c.1516dup ENSP00000513996.1:p.Arg506ProfsTer?
ENST00000698871.1:n.2039dup
ENST00000698872.1:c.*305dup ENSP00000513997.1:n.*305dup
ENST00000698873.1:c.*711dup ENSP00000513998.1:n.*711dup
ENST00000698874.1:c.976dup ENSP00000513999.1:p.Arg326ProfsTer?
ENST00000698875.1:n.1376dup
ENST00000698876.1:n.1564dup
ENST00000698877.1:n.1084dup
ENST00000698878.1:c.1510dup ENSP00000514000.1:p.Arg504ProfsTer?
ENST00000698880.1:c.1384dup
ENST00000345728.10:c.1516dup MANE Select ENSP00000339950.5:p.Arg506ProfsTer?
ENST00000279227.9:c.1528dup ENSP00000279227.5:p.Arg510ProfsTer?
ENST00000345728.9:c.1516dup ENSP00000339950.5:p.Arg506ProfsTer?
ENST00000545896.1:c.204dup ENSP00000440209.1:p.Val69ArgfsTer?
NM_031471.5:c.1516dup NP_113659.3:p.Arg506ProfsTer?
NM_178443.2:c.1528dup , LRG_180t1:c.1528dup NP_848537.1:p.Arg510ProfsTer?
XM_011545294.1:c.1528dup XP_011543596.1:p.Arg510ProfsTer?
XM_011545295.1:c.988dup XP_011543597.1:p.Arg330ProfsTer?
XM_011545296.1:c.988dup XP_011543598.1:p.Arg330ProfsTer?
XM_011545294.3:c.1528dup XP_011543596.1:p.Arg510ProfsTer?
XM_011545295.2:c.988dup XP_011543597.1:p.Arg330ProfsTer?
XM_017018398.2:c.1516dup XP_016873887.1:p.Arg506ProfsTer?
XM_017018399.1:c.976dup XP_016873888.1:p.Arg326ProfsTer?
NM_031471.6:c.1516dup MANE Select NP_113659.3:p.Arg506ProfsTer?
NM_001382361.1:c.1516dup NP_001369290.1:p.Arg506ProfsTer?
NM_001382362.1:c.1528dup NP_001369291.1:p.Arg510ProfsTer?
NM_001382363.1:c.976dup NP_001369292.1:p.Arg326ProfsTer?
NM_001382364.1:c.988dup NP_001369293.1:p.Arg330ProfsTer?
NM_001382448.1:c.1516dup NP_001369377.1:p.Arg506ProfsTer?
NM_178443.3:c.1528dup NP_848537.1:p.Arg510ProfsTer?