Canonical Allele Identifier: CA1978639134
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220580C= , CM000673.2:g.64220580C= GRCh38
NC_000011.9:g.63988052C= , CM000673.1:g.63988052C= GRCh37
NC_000011.8:g.63744628C= NCBI36
NG_016360.1:g.18901C= , LRG_180:g.18901C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1468C= ENSP00000279227.5:p.His490=
ENST00000540554.2:n.2634C=
ENST00000541252.2:c.916C= ENSP00000438885.2:p.His306=
ENST00000541326.6:n.877C=
ENST00000544997.6:c.1456C= ENSP00000445778.2:p.His486=
ENST00000545896.2:c.145C= ENSP00000440209.2:p.His49=
ENST00000546255.2:n.1760C=
ENST00000698845.1:c.*651C= ENSP00000513981.1:n.*651C=
ENST00000698846.1:n.1702C=
ENST00000698847.1:c.*861C= ENSP00000513982.1:n.*861C=
ENST00000698849.1:n.576C=
ENST00000698850.1:n.1224C=
ENST00000698852.1:c.1456C= ENSP00000513984.1:p.His486=
ENST00000698853.1:c.*685C= ENSP00000513985.1:n.*685C=
ENST00000698854.1:c.*786C= ENSP00000513986.1:n.*786C=
ENST00000698855.1:n.3108C=
ENST00000698856.1:n.2802C=
ENST00000698859.1:n.1620C=
ENST00000698860.1:c.1468C= ENSP00000513988.1:p.His490=
ENST00000698861.1:c.1456C= ENSP00000513989.1:p.His486=
ENST00000698862.1:c.*752C= ENSP00000513990.1:n.*752C=
ENST00000698863.1:c.1456C= ENSP00000513991.1:p.His486=
ENST00000698864.1:n.1671C=
ENST00000698865.1:c.1477C= ENSP00000513992.1:p.His493=
ENST00000698866.1:c.*970C= ENSP00000513993.1:n.*970C=
ENST00000698867.1:n.5431C=
ENST00000698868.1:c.1321C= ENSP00000513994.1:p.His441=
ENST00000698869.1:c.1311+254C= ENSP00000513995.1:n.1311+254C=
ENST00000698870.1:c.1456C= ENSP00000513996.1:p.His486=
ENST00000698871.1:n.1979C=
ENST00000698872.1:c.*245C= ENSP00000513997.1:n.*245C=
ENST00000698873.1:c.*651C= ENSP00000513998.1:n.*651C=
ENST00000698874.1:c.916C= ENSP00000513999.1:p.His306=
ENST00000698875.1:n.1316C=
ENST00000698876.1:n.1504C=
ENST00000698877.1:n.1024C=
ENST00000698878.1:c.1450C= ENSP00000514000.1:p.His484=
ENST00000698880.1:c.1324C=
ENST00000345728.10:c.1456C= MANE Select ENSP00000339950.5:p.His486=
ENST00000279227.9:c.1468C= ENSP00000279227.5:p.His490=
ENST00000345728.9:c.1456C= ENSP00000339950.5:p.His486=
ENST00000541326.5:n.872C=
ENST00000545896.1:c.144C= ENSP00000440209.1:p.Thr48=
NM_031471.5:c.1456C= NP_113659.3:p.His486=
NM_178443.2:c.1468C= , LRG_180t1:c.1468C= NP_848537.1:p.His490=
XM_011545294.1:c.1468C= XP_011543596.1:p.His490=
XM_011545295.1:c.928C= XP_011543597.1:p.His310=
XM_011545296.1:c.928C= XP_011543598.1:p.His310=
XM_011545294.3:c.1468C= XP_011543596.1:p.His490=
XM_011545295.2:c.928C= XP_011543597.1:p.His310=
XM_017018398.2:c.1456C= XP_016873887.1:p.His486=
XM_017018399.1:c.916C= XP_016873888.1:p.His306=
NM_031471.6:c.1456C= MANE Select NP_113659.3:p.His486=
NM_001382361.1:c.1456C= NP_001369290.1:p.His486=
NM_001382362.1:c.1468C= NP_001369291.1:p.His490=
NM_001382363.1:c.916C= NP_001369292.1:p.His306=
NM_001382364.1:c.928C= NP_001369293.1:p.His310=
NM_001382448.1:c.1456C= NP_001369377.1:p.His486=
NM_178443.3:c.1468C= NP_848537.1:p.His490=