Canonical Allele Identifier: CA1978639091
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220557C= , CM000673.2:g.64220557C= GRCh38
NC_000011.9:g.63988029C= , CM000673.1:g.63988029C= GRCh37
NC_000011.8:g.63744605C= NCBI36
NG_016360.1:g.18878C= , LRG_180:g.18878C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1445C= ENSP00000279227.5:p.Thr482=
ENST00000540554.2:n.2611C=
ENST00000541252.2:c.893C= ENSP00000438885.2:p.Thr298=
ENST00000541326.6:n.854C=
ENST00000544997.6:c.1433C= ENSP00000445778.2:p.Thr478=
ENST00000545896.2:c.122C= ENSP00000440209.2:p.Thr41=
ENST00000546255.2:n.1737C=
ENST00000698845.1:c.*628C= ENSP00000513981.1:n.*628C=
ENST00000698846.1:n.1679C=
ENST00000698847.1:c.*838C= ENSP00000513982.1:n.*838C=
ENST00000698849.1:n.553C=
ENST00000698850.1:n.1201C=
ENST00000698852.1:c.1433C= ENSP00000513984.1:p.Thr478=
ENST00000698853.1:c.*662C= ENSP00000513985.1:n.*662C=
ENST00000698854.1:c.*763C= ENSP00000513986.1:n.*763C=
ENST00000698855.1:n.3085C=
ENST00000698856.1:n.2779C=
ENST00000698859.1:n.1597C=
ENST00000698860.1:c.1445C= ENSP00000513988.1:p.Thr482=
ENST00000698861.1:c.1433C= ENSP00000513989.1:p.Thr478=
ENST00000698862.1:c.*729C= ENSP00000513990.1:n.*729C=
ENST00000698863.1:c.1433C= ENSP00000513991.1:p.Thr478=
ENST00000698864.1:n.1648C=
ENST00000698865.1:c.1454C= ENSP00000513992.1:p.Thr485=
ENST00000698866.1:c.*947C= ENSP00000513993.1:n.*947C=
ENST00000698867.1:n.5408C=
ENST00000698868.1:c.1298C= ENSP00000513994.1:p.Thr433=
ENST00000698869.1:c.1311+231C= ENSP00000513995.1:n.1311+231C=
ENST00000698870.1:c.1433C= ENSP00000513996.1:p.Thr478=
ENST00000698871.1:n.1956C=
ENST00000698872.1:c.*222C= ENSP00000513997.1:n.*222C=
ENST00000698873.1:c.*628C= ENSP00000513998.1:n.*628C=
ENST00000698874.1:c.893C= ENSP00000513999.1:p.Thr298=
ENST00000698875.1:n.1293C=
ENST00000698876.1:n.1481C=
ENST00000698877.1:n.1001C=
ENST00000698878.1:c.1427C= ENSP00000514000.1:p.Thr476=
ENST00000698880.1:c.1301C=
ENST00000345728.10:c.1433C= MANE Select ENSP00000339950.5:p.Thr478=
ENST00000279227.9:c.1445C= ENSP00000279227.5:p.Thr482=
ENST00000345728.9:c.1433C= ENSP00000339950.5:p.Thr478=
ENST00000541326.5:n.849C=
ENST00000545896.1:c.121C= ENSP00000440209.1:p.Arg41=
NM_031471.5:c.1433C= NP_113659.3:p.Thr478=
NM_178443.2:c.1445C= , LRG_180t1:c.1445C= NP_848537.1:p.Thr482=
XM_011545294.1:c.1445C= XP_011543596.1:p.Thr482=
XM_011545295.1:c.905C= XP_011543597.1:p.Thr302=
XM_011545296.1:c.905C= XP_011543598.1:p.Thr302=
XM_011545294.3:c.1445C= XP_011543596.1:p.Thr482=
XM_011545295.2:c.905C= XP_011543597.1:p.Thr302=
XM_017018398.2:c.1433C= XP_016873887.1:p.Thr478=
XM_017018399.1:c.893C= XP_016873888.1:p.Thr298=
NM_031471.6:c.1433C= MANE Select NP_113659.3:p.Thr478=
NM_001382361.1:c.1433C= NP_001369290.1:p.Thr478=
NM_001382362.1:c.1445C= NP_001369291.1:p.Thr482=
NM_001382363.1:c.893C= NP_001369292.1:p.Thr298=
NM_001382364.1:c.905C= NP_001369293.1:p.Thr302=
NM_001382448.1:c.1433C= NP_001369377.1:p.Thr478=
NM_178443.3:c.1445C= NP_848537.1:p.Thr482=