Canonical Allele Identifier: CA1978638932
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220489C= , CM000673.2:g.64220489C= GRCh38
NC_000011.9:g.63987961C= , CM000673.1:g.63987961C= GRCh37
NC_000011.8:g.63744537C= NCBI36
NG_016360.1:g.18810C= , LRG_180:g.18810C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1377C= ENSP00000279227.5:p.Arg459=
ENST00000540554.2:n.2543C=
ENST00000541252.2:c.825C= ENSP00000438885.2:p.Arg275=
ENST00000541326.6:n.786C=
ENST00000544997.6:c.1365C= ENSP00000445778.2:p.Arg455=
ENST00000545896.2:c.54C= ENSP00000440209.2:p.Arg18=
ENST00000546255.2:n.1669C=
ENST00000698845.1:c.*560C= ENSP00000513981.1:n.*560C=
ENST00000698846.1:n.1611C=
ENST00000698847.1:c.*770C= ENSP00000513982.1:n.*770C=
ENST00000698849.1:n.485C=
ENST00000698850.1:n.1133C=
ENST00000698852.1:c.1365C= ENSP00000513984.1:p.Arg455=
ENST00000698853.1:c.*594C= ENSP00000513985.1:n.*594C=
ENST00000698854.1:c.*695C= ENSP00000513986.1:n.*695C=
ENST00000698855.1:n.3017C=
ENST00000698856.1:n.2711C=
ENST00000698859.1:n.1529C=
ENST00000698860.1:c.1377C= ENSP00000513988.1:p.Arg459=
ENST00000698861.1:c.1365C= ENSP00000513989.1:p.Arg455=
ENST00000698862.1:c.*661C= ENSP00000513990.1:n.*661C=
ENST00000698863.1:c.1365C= ENSP00000513991.1:p.Arg455=
ENST00000698864.1:n.1580C=
ENST00000698865.1:c.1386C= ENSP00000513992.1:p.Arg462=
ENST00000698866.1:c.*879C= ENSP00000513993.1:n.*879C=
ENST00000698867.1:n.5340C=
ENST00000698868.1:c.1230C= ENSP00000513994.1:p.Arg410=
ENST00000698869.1:c.1311+163C= ENSP00000513995.1:n.1311+163C=
ENST00000698870.1:c.1365C= ENSP00000513996.1:p.Arg455=
ENST00000698871.1:n.1888C=
ENST00000698872.1:c.*154C= ENSP00000513997.1:n.*154C=
ENST00000698873.1:c.*560C= ENSP00000513998.1:n.*560C=
ENST00000698874.1:c.825C= ENSP00000513999.1:p.Arg275=
ENST00000698875.1:n.1225C=
ENST00000698876.1:n.1413C=
ENST00000698877.1:n.933C=
ENST00000698878.1:c.1359C= ENSP00000514000.1:p.Arg453=
ENST00000698880.1:c.1233C=
ENST00000345728.10:c.1365C= MANE Select ENSP00000339950.5:p.Arg455=
ENST00000279227.9:c.1377C= ENSP00000279227.5:p.Arg459=
ENST00000345728.9:c.1365C= ENSP00000339950.5:p.Arg455=
ENST00000541326.5:n.781C=
ENST00000545896.1:c.53C= ENSP00000440209.1:p.Ala18=
NM_031471.5:c.1365C= NP_113659.3:p.Arg455=
NM_178443.2:c.1377C= , LRG_180t1:c.1377C= NP_848537.1:p.Arg459=
XM_011545294.1:c.1377C= XP_011543596.1:p.Arg459=
XM_011545295.1:c.837C= XP_011543597.1:p.Arg279=
XM_011545296.1:c.837C= XP_011543598.1:p.Arg279=
XM_011545294.3:c.1377C= XP_011543596.1:p.Arg459=
XM_011545295.2:c.837C= XP_011543597.1:p.Arg279=
XM_017018398.2:c.1365C= XP_016873887.1:p.Arg455=
XM_017018399.1:c.825C= XP_016873888.1:p.Arg275=
NM_031471.6:c.1365C= MANE Select NP_113659.3:p.Arg455=
NM_001382361.1:c.1365C= NP_001369290.1:p.Arg455=
NM_001382362.1:c.1377C= NP_001369291.1:p.Arg459=
NM_001382363.1:c.825C= NP_001369292.1:p.Arg275=
NM_001382364.1:c.837C= NP_001369293.1:p.Arg279=
NM_001382448.1:c.1365C= NP_001369377.1:p.Arg455=
NM_178443.3:c.1377C= NP_848537.1:p.Arg459=