Canonical Allele Identifier: CA1978639262
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220649C= , CM000673.2:g.64220649C= GRCh38
NC_000011.9:g.63988121C= , CM000673.1:g.63988121C= GRCh37
NC_000011.8:g.63744697C= NCBI36
NG_016360.1:g.18970C= , LRG_180:g.18970C=

Transcript Alleles

HGVS Amino-acid change
ENST00000279227.10:c.1537C= ENSP00000279227.5:p.Arg513=
ENST00000540554.2:n.2703C=
ENST00000541252.2:c.985C= ENSP00000438885.2:p.Arg329=
ENST00000541326.6:n.946C=
ENST00000544997.6:c.1525C= ENSP00000445778.2:p.Arg509=
ENST00000545896.2:c.214C= ENSP00000440209.2:p.Arg72=
ENST00000546255.2:n.1829C=
ENST00000698845.1:c.*720C= ENSP00000513981.1:n.*720C=
ENST00000698846.1:n.1771C=
ENST00000698847.1:c.*930C= ENSP00000513982.1:n.*930C=
ENST00000698849.1:n.645C=
ENST00000698850.1:n.1293C=
ENST00000698852.1:c.1525C= ENSP00000513984.1:p.Arg509=
ENST00000698853.1:c.*754C= ENSP00000513985.1:n.*754C=
ENST00000698854.1:c.*855C= ENSP00000513986.1:n.*855C=
ENST00000698855.1:n.3177C=
ENST00000698856.1:n.2871C=
ENST00000698859.1:n.1689C=
ENST00000698860.1:c.1537C= ENSP00000513988.1:p.Arg513=
ENST00000698861.1:c.1525C= ENSP00000513989.1:p.Arg509=
ENST00000698862.1:c.*821C= ENSP00000513990.1:n.*821C=
ENST00000698863.1:c.1525C= ENSP00000513991.1:p.Arg509=
ENST00000698864.1:n.1740C=
ENST00000698865.1:c.1546C= ENSP00000513992.1:p.Arg516=
ENST00000698866.1:c.*1039C= ENSP00000513993.1:n.*1039C=
ENST00000698867.1:n.5500C=
ENST00000698868.1:c.1390C= ENSP00000513994.1:p.Arg464=
ENST00000698869.1:c.1311+323C= ENSP00000513995.1:n.1311+323C=
ENST00000698870.1:c.1525C= ENSP00000513996.1:p.Arg509=
ENST00000698871.1:n.2048C=
ENST00000698872.1:c.*314C= ENSP00000513997.1:n.*314C=
ENST00000698873.1:c.*720C= ENSP00000513998.1:n.*720C=
ENST00000698874.1:c.985C= ENSP00000513999.1:p.Arg329=
ENST00000698875.1:n.1385C=
ENST00000698876.1:n.1573C=
ENST00000698877.1:n.1093C=
ENST00000698878.1:c.1519C= ENSP00000514000.1:p.Arg507=
ENST00000698880.1:c.1393C=
ENST00000345728.10:c.1525C= MANE Select ENSP00000339950.5:p.Arg509=
ENST00000279227.9:c.1537C= ENSP00000279227.5:p.Arg513=
ENST00000345728.9:c.1525C= ENSP00000339950.5:p.Arg509=
ENST00000545896.1:c.213C= ENSP00000440209.1:p.Ser71=
NM_031471.5:c.1525C= NP_113659.3:p.Arg509=
NM_178443.2:c.1537C= , LRG_180t1:c.1537C= NP_848537.1:p.Arg513=
XM_011545294.1:c.1537C= XP_011543596.1:p.Arg513=
XM_011545295.1:c.997C= XP_011543597.1:p.Arg333=
XM_011545296.1:c.997C= XP_011543598.1:p.Arg333=
XM_011545294.3:c.1537C= XP_011543596.1:p.Arg513=
XM_011545295.2:c.997C= XP_011543597.1:p.Arg333=
XM_017018398.2:c.1525C= XP_016873887.1:p.Arg509=
XM_017018399.1:c.985C= XP_016873888.1:p.Arg329=
NM_031471.6:c.1525C= MANE Select NP_113659.3:p.Arg509=
NM_001382361.1:c.1525C= NP_001369290.1:p.Arg509=
NM_001382362.1:c.1537C= NP_001369291.1:p.Arg513=
NM_001382363.1:c.985C= NP_001369292.1:p.Arg329=
NM_001382364.1:c.997C= NP_001369293.1:p.Arg333=
NM_001382448.1:c.1525C= NP_001369377.1:p.Arg509=
NM_178443.3:c.1537C= NP_848537.1:p.Arg513=