Canonical Allele Identifier: CA1978639241
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220638C= , CM000673.2:g.64220638C= GRCh38
NC_000011.9:g.63988110C= , CM000673.1:g.63988110C= GRCh37
NC_000011.8:g.63744686C= NCBI36
NG_016360.1:g.18959C= , LRG_180:g.18959C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1526C= ENSP00000279227.5:p.Pro509=
ENST00000540554.2:n.2692C=
ENST00000541252.2:c.974C= ENSP00000438885.2:p.Pro325=
ENST00000541326.6:n.935C=
ENST00000544997.6:c.1514C= ENSP00000445778.2:p.Pro505=
ENST00000545896.2:c.203C= ENSP00000440209.2:p.Pro68=
ENST00000546255.2:n.1818C=
ENST00000698845.1:c.*709C= ENSP00000513981.1:n.*709C=
ENST00000698846.1:n.1760C=
ENST00000698847.1:c.*919C= ENSP00000513982.1:n.*919C=
ENST00000698849.1:n.634C=
ENST00000698850.1:n.1282C=
ENST00000698852.1:c.1514C= ENSP00000513984.1:p.Pro505=
ENST00000698853.1:c.*743C= ENSP00000513985.1:n.*743C=
ENST00000698854.1:c.*844C= ENSP00000513986.1:n.*844C=
ENST00000698855.1:n.3166C=
ENST00000698856.1:n.2860C=
ENST00000698859.1:n.1678C=
ENST00000698860.1:c.1526C= ENSP00000513988.1:p.Pro509=
ENST00000698861.1:c.1514C= ENSP00000513989.1:p.Pro505=
ENST00000698862.1:c.*810C= ENSP00000513990.1:n.*810C=
ENST00000698863.1:c.1514C= ENSP00000513991.1:p.Pro505=
ENST00000698864.1:n.1729C=
ENST00000698865.1:c.1535C= ENSP00000513992.1:p.Pro512=
ENST00000698866.1:c.*1028C= ENSP00000513993.1:n.*1028C=
ENST00000698867.1:n.5489C=
ENST00000698868.1:c.1379C= ENSP00000513994.1:p.Pro460=
ENST00000698869.1:c.1311+312C= ENSP00000513995.1:n.1311+312C=
ENST00000698870.1:c.1514C= ENSP00000513996.1:p.Pro505=
ENST00000698871.1:n.2037C=
ENST00000698872.1:c.*303C= ENSP00000513997.1:n.*303C=
ENST00000698873.1:c.*709C= ENSP00000513998.1:n.*709C=
ENST00000698874.1:c.974C= ENSP00000513999.1:p.Pro325=
ENST00000698875.1:n.1374C=
ENST00000698876.1:n.1562C=
ENST00000698877.1:n.1082C=
ENST00000698878.1:c.1508C= ENSP00000514000.1:p.Pro503=
ENST00000698880.1:c.1382C=
ENST00000345728.10:c.1514C= MANE Select ENSP00000339950.5:p.Pro505=
ENST00000279227.9:c.1526C= ENSP00000279227.5:p.Pro509=
ENST00000345728.9:c.1514C= ENSP00000339950.5:p.Pro505=
ENST00000545896.1:c.202C= ENSP00000440209.1:p.Pro68=
NM_031471.5:c.1514C= NP_113659.3:p.Pro505=
NM_178443.2:c.1526C= , LRG_180t1:c.1526C= NP_848537.1:p.Pro509=
XM_011545294.1:c.1526C= XP_011543596.1:p.Pro509=
XM_011545295.1:c.986C= XP_011543597.1:p.Pro329=
XM_011545296.1:c.986C= XP_011543598.1:p.Pro329=
XM_011545294.3:c.1526C= XP_011543596.1:p.Pro509=
XM_011545295.2:c.986C= XP_011543597.1:p.Pro329=
XM_017018398.2:c.1514C= XP_016873887.1:p.Pro505=
XM_017018399.1:c.974C= XP_016873888.1:p.Pro325=
NM_031471.6:c.1514C= MANE Select NP_113659.3:p.Pro505=
NM_001382361.1:c.1514C= NP_001369290.1:p.Pro505=
NM_001382362.1:c.1526C= NP_001369291.1:p.Pro509=
NM_001382363.1:c.974C= NP_001369292.1:p.Pro325=
NM_001382364.1:c.986C= NP_001369293.1:p.Pro329=
NM_001382448.1:c.1514C= NP_001369377.1:p.Pro505=
NM_178443.3:c.1526C= NP_848537.1:p.Pro509=