Canonical Allele Identifier: CA1978638888
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220469C= , CM000673.2:g.64220469C= GRCh38
NC_000011.9:g.63987941C= , CM000673.1:g.63987941C= GRCh37
NC_000011.8:g.63744517C= NCBI36
NG_016360.1:g.18790C= , LRG_180:g.18790C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1357C= ENSP00000279227.5:p.Arg453=
ENST00000540554.2:n.2523C=
ENST00000541252.2:c.805C= ENSP00000438885.2:p.Arg269=
ENST00000541326.6:n.766C=
ENST00000544997.6:c.1345C= ENSP00000445778.2:p.Arg449=
ENST00000545896.2:c.34C= ENSP00000440209.2:p.Arg12=
ENST00000546255.2:n.1649C=
ENST00000698845.1:c.*540C= ENSP00000513981.1:n.*540C=
ENST00000698846.1:n.1591C=
ENST00000698847.1:c.*750C= ENSP00000513982.1:n.*750C=
ENST00000698848.1:n.643C=
ENST00000698849.1:n.465C=
ENST00000698850.1:n.1113C=
ENST00000698852.1:c.1345C= ENSP00000513984.1:p.Arg449=
ENST00000698853.1:c.*574C= ENSP00000513985.1:n.*574C=
ENST00000698854.1:c.*675C= ENSP00000513986.1:n.*675C=
ENST00000698855.1:n.2997C=
ENST00000698856.1:n.2691C=
ENST00000698859.1:n.1509C=
ENST00000698860.1:c.1357C= ENSP00000513988.1:p.Arg453=
ENST00000698861.1:c.1345C= ENSP00000513989.1:p.Arg449=
ENST00000698862.1:c.*641C= ENSP00000513990.1:n.*641C=
ENST00000698863.1:c.1345C= ENSP00000513991.1:p.Arg449=
ENST00000698864.1:n.1560C=
ENST00000698865.1:c.1366C= ENSP00000513992.1:p.Arg456=
ENST00000698866.1:c.*859C= ENSP00000513993.1:n.*859C=
ENST00000698867.1:n.5320C=
ENST00000698868.1:c.1210C= ENSP00000513994.1:p.Arg404=
ENST00000698869.1:c.1311+143C= ENSP00000513995.1:n.1311+143C=
ENST00000698870.1:c.1345C= ENSP00000513996.1:p.Arg449=
ENST00000698871.1:n.1868C=
ENST00000698872.1:c.*134C= ENSP00000513997.1:n.*134C=
ENST00000698873.1:c.*540C= ENSP00000513998.1:n.*540C=
ENST00000698874.1:c.805C= ENSP00000513999.1:p.Arg269=
ENST00000698875.1:n.1205C=
ENST00000698876.1:n.1393C=
ENST00000698877.1:n.913C=
ENST00000698878.1:c.1339C= ENSP00000514000.1:p.Arg447=
ENST00000698880.1:c.1213C=
ENST00000345728.10:c.1345C= MANE Select ENSP00000339950.5:p.Arg449=
ENST00000279227.9:c.1357C= ENSP00000279227.5:p.Arg453=
ENST00000345728.9:c.1345C= ENSP00000339950.5:p.Arg449=
ENST00000541326.5:n.761C=
ENST00000545896.1:c.33C= ENSP00000440209.1:p.Ala11=
NM_031471.5:c.1345C= NP_113659.3:p.Arg449=
NM_178443.2:c.1357C= , LRG_180t1:c.1357C= NP_848537.1:p.Arg453=
XM_011545294.1:c.1357C= XP_011543596.1:p.Arg453=
XM_011545295.1:c.817C= XP_011543597.1:p.Arg273=
XM_011545296.1:c.817C= XP_011543598.1:p.Arg273=
XM_011545294.3:c.1357C= XP_011543596.1:p.Arg453=
XM_011545295.2:c.817C= XP_011543597.1:p.Arg273=
XM_017018398.2:c.1345C= XP_016873887.1:p.Arg449=
XM_017018399.1:c.805C= XP_016873888.1:p.Arg269=
NM_031471.6:c.1345C= MANE Select NP_113659.3:p.Arg449=
NM_001382361.1:c.1345C= NP_001369290.1:p.Arg449=
NM_001382362.1:c.1357C= NP_001369291.1:p.Arg453=
NM_001382363.1:c.805C= NP_001369292.1:p.Arg269=
NM_001382364.1:c.817C= NP_001369293.1:p.Arg273=
NM_001382448.1:c.1345C= NP_001369377.1:p.Arg449=
NM_178443.3:c.1357C= NP_848537.1:p.Arg453=