Canonical Allele Identifier: CA1978638926
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220487C= , CM000673.2:g.64220487C= GRCh38
NC_000011.9:g.63987959C= , CM000673.1:g.63987959C= GRCh37
NC_000011.8:g.63744535C= NCBI36
NG_016360.1:g.18808C= , LRG_180:g.18808C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1375C= ENSP00000279227.5:p.Arg459=
ENST00000540554.2:n.2541C=
ENST00000541252.2:c.823C= ENSP00000438885.2:p.Arg275=
ENST00000541326.6:n.784C=
ENST00000544997.6:c.1363C= ENSP00000445778.2:p.Arg455=
ENST00000545896.2:c.52C= ENSP00000440209.2:p.Arg18=
ENST00000546255.2:n.1667C=
ENST00000698845.1:c.*558C= ENSP00000513981.1:n.*558C=
ENST00000698846.1:n.1609C=
ENST00000698847.1:c.*768C= ENSP00000513982.1:n.*768C=
ENST00000698849.1:n.483C=
ENST00000698850.1:n.1131C=
ENST00000698852.1:c.1363C= ENSP00000513984.1:p.Arg455=
ENST00000698853.1:c.*592C= ENSP00000513985.1:n.*592C=
ENST00000698854.1:c.*693C= ENSP00000513986.1:n.*693C=
ENST00000698855.1:n.3015C=
ENST00000698856.1:n.2709C=
ENST00000698859.1:n.1527C=
ENST00000698860.1:c.1375C= ENSP00000513988.1:p.Arg459=
ENST00000698861.1:c.1363C= ENSP00000513989.1:p.Arg455=
ENST00000698862.1:c.*659C= ENSP00000513990.1:n.*659C=
ENST00000698863.1:c.1363C= ENSP00000513991.1:p.Arg455=
ENST00000698864.1:n.1578C=
ENST00000698865.1:c.1384C= ENSP00000513992.1:p.Arg462=
ENST00000698866.1:c.*877C= ENSP00000513993.1:n.*877C=
ENST00000698867.1:n.5338C=
ENST00000698868.1:c.1228C= ENSP00000513994.1:p.Arg410=
ENST00000698869.1:c.1311+161C= ENSP00000513995.1:n.1311+161C=
ENST00000698870.1:c.1363C= ENSP00000513996.1:p.Arg455=
ENST00000698871.1:n.1886C=
ENST00000698872.1:c.*152C= ENSP00000513997.1:n.*152C=
ENST00000698873.1:c.*558C= ENSP00000513998.1:n.*558C=
ENST00000698874.1:c.823C= ENSP00000513999.1:p.Arg275=
ENST00000698875.1:n.1223C=
ENST00000698876.1:n.1411C=
ENST00000698877.1:n.931C=
ENST00000698878.1:c.1357C= ENSP00000514000.1:p.Arg453=
ENST00000698880.1:c.1231C=
ENST00000345728.10:c.1363C= MANE Select ENSP00000339950.5:p.Arg455=
ENST00000279227.9:c.1375C= ENSP00000279227.5:p.Arg459=
ENST00000345728.9:c.1363C= ENSP00000339950.5:p.Arg455=
ENST00000541326.5:n.779C=
ENST00000545896.1:c.51C= ENSP00000440209.1:p.Ala17=
NM_031471.5:c.1363C= NP_113659.3:p.Arg455=
NM_178443.2:c.1375C= , LRG_180t1:c.1375C= NP_848537.1:p.Arg459=
XM_011545294.1:c.1375C= XP_011543596.1:p.Arg459=
XM_011545295.1:c.835C= XP_011543597.1:p.Arg279=
XM_011545296.1:c.835C= XP_011543598.1:p.Arg279=
XM_011545294.3:c.1375C= XP_011543596.1:p.Arg459=
XM_011545295.2:c.835C= XP_011543597.1:p.Arg279=
XM_017018398.2:c.1363C= XP_016873887.1:p.Arg455=
XM_017018399.1:c.823C= XP_016873888.1:p.Arg275=
NM_031471.6:c.1363C= MANE Select NP_113659.3:p.Arg455=
NM_001382361.1:c.1363C= NP_001369290.1:p.Arg455=
NM_001382362.1:c.1375C= NP_001369291.1:p.Arg459=
NM_001382363.1:c.823C= NP_001369292.1:p.Arg275=
NM_001382364.1:c.835C= NP_001369293.1:p.Arg279=
NM_001382448.1:c.1363C= NP_001369377.1:p.Arg455=
NM_178443.3:c.1375C= NP_848537.1:p.Arg459=