Canonical Allele Identifier: CA1978639142
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220583C= , CM000673.2:g.64220583C= GRCh38
NC_000011.9:g.63988055C= , CM000673.1:g.63988055C= GRCh37
NC_000011.8:g.63744631C= NCBI36
NG_016360.1:g.18904C= , LRG_180:g.18904C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1471C= ENSP00000279227.5:p.Pro491=
ENST00000540554.2:n.2637C=
ENST00000541252.2:c.919C= ENSP00000438885.2:p.Pro307=
ENST00000541326.6:n.880C=
ENST00000544997.6:c.1459C= ENSP00000445778.2:p.Pro487=
ENST00000545896.2:c.148C= ENSP00000440209.2:p.Pro50=
ENST00000546255.2:n.1763C=
ENST00000698845.1:c.*654C= ENSP00000513981.1:n.*654C=
ENST00000698846.1:n.1705C=
ENST00000698847.1:c.*864C= ENSP00000513982.1:n.*864C=
ENST00000698849.1:n.579C=
ENST00000698850.1:n.1227C=
ENST00000698852.1:c.1459C= ENSP00000513984.1:p.Pro487=
ENST00000698853.1:c.*688C= ENSP00000513985.1:n.*688C=
ENST00000698854.1:c.*789C= ENSP00000513986.1:n.*789C=
ENST00000698855.1:n.3111C=
ENST00000698856.1:n.2805C=
ENST00000698859.1:n.1623C=
ENST00000698860.1:c.1471C= ENSP00000513988.1:p.Pro491=
ENST00000698861.1:c.1459C= ENSP00000513989.1:p.Pro487=
ENST00000698862.1:c.*755C= ENSP00000513990.1:n.*755C=
ENST00000698863.1:c.1459C= ENSP00000513991.1:p.Pro487=
ENST00000698864.1:n.1674C=
ENST00000698865.1:c.1480C= ENSP00000513992.1:p.Pro494=
ENST00000698866.1:c.*973C= ENSP00000513993.1:n.*973C=
ENST00000698867.1:n.5434C=
ENST00000698868.1:c.1324C= ENSP00000513994.1:p.Pro442=
ENST00000698869.1:c.1311+257C= ENSP00000513995.1:n.1311+257C=
ENST00000698870.1:c.1459C= ENSP00000513996.1:p.Pro487=
ENST00000698871.1:n.1982C=
ENST00000698872.1:c.*248C= ENSP00000513997.1:n.*248C=
ENST00000698873.1:c.*654C= ENSP00000513998.1:n.*654C=
ENST00000698874.1:c.919C= ENSP00000513999.1:p.Pro307=
ENST00000698875.1:n.1319C=
ENST00000698876.1:n.1507C=
ENST00000698877.1:n.1027C=
ENST00000698878.1:c.1453C= ENSP00000514000.1:p.Pro485=
ENST00000698880.1:c.1327C=
ENST00000345728.10:c.1459C= MANE Select ENSP00000339950.5:p.Pro487=
ENST00000279227.9:c.1471C= ENSP00000279227.5:p.Pro491=
ENST00000345728.9:c.1459C= ENSP00000339950.5:p.Pro487=
ENST00000541326.5:n.875C=
ENST00000545896.1:c.147C= ENSP00000440209.1:p.Thr49=
NM_031471.5:c.1459C= NP_113659.3:p.Pro487=
NM_178443.2:c.1471C= , LRG_180t1:c.1471C= NP_848537.1:p.Pro491=
XM_011545294.1:c.1471C= XP_011543596.1:p.Pro491=
XM_011545295.1:c.931C= XP_011543597.1:p.Pro311=
XM_011545296.1:c.931C= XP_011543598.1:p.Pro311=
XM_011545294.3:c.1471C= XP_011543596.1:p.Pro491=
XM_011545295.2:c.931C= XP_011543597.1:p.Pro311=
XM_017018398.2:c.1459C= XP_016873887.1:p.Pro487=
XM_017018399.1:c.919C= XP_016873888.1:p.Pro307=
NM_031471.6:c.1459C= MANE Select NP_113659.3:p.Pro487=
NM_001382361.1:c.1459C= NP_001369290.1:p.Pro487=
NM_001382362.1:c.1471C= NP_001369291.1:p.Pro491=
NM_001382363.1:c.919C= NP_001369292.1:p.Pro307=
NM_001382364.1:c.931C= NP_001369293.1:p.Pro311=
NM_001382448.1:c.1459C= NP_001369377.1:p.Pro487=
NM_178443.3:c.1471C= NP_848537.1:p.Pro491=