Canonical Allele Identifier: CA1978639213
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220627C= , CM000673.2:g.64220627C= GRCh38
NC_000011.9:g.63988099C= , CM000673.1:g.63988099C= GRCh37
NC_000011.8:g.63744675C= NCBI36
NG_016360.1:g.18948C= , LRG_180:g.18948C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1515C= ENSP00000279227.5:p.Gly505=
ENST00000540554.2:n.2681C=
ENST00000541252.2:c.963C= ENSP00000438885.2:p.Gly321=
ENST00000541326.6:n.924C=
ENST00000544997.6:c.1503C= ENSP00000445778.2:p.Gly501=
ENST00000545896.2:c.192C= ENSP00000440209.2:p.Gly64=
ENST00000546255.2:n.1807C=
ENST00000698845.1:c.*698C= ENSP00000513981.1:n.*698C=
ENST00000698846.1:n.1749C=
ENST00000698847.1:c.*908C= ENSP00000513982.1:n.*908C=
ENST00000698849.1:n.623C=
ENST00000698850.1:n.1271C=
ENST00000698852.1:c.1503C= ENSP00000513984.1:p.Gly501=
ENST00000698853.1:c.*732C= ENSP00000513985.1:n.*732C=
ENST00000698854.1:c.*833C= ENSP00000513986.1:n.*833C=
ENST00000698855.1:n.3155C=
ENST00000698856.1:n.2849C=
ENST00000698859.1:n.1667C=
ENST00000698860.1:c.1515C= ENSP00000513988.1:p.Gly505=
ENST00000698861.1:c.1503C= ENSP00000513989.1:p.Gly501=
ENST00000698862.1:c.*799C= ENSP00000513990.1:n.*799C=
ENST00000698863.1:c.1503C= ENSP00000513991.1:p.Gly501=
ENST00000698864.1:n.1718C=
ENST00000698865.1:c.1524C= ENSP00000513992.1:p.Gly508=
ENST00000698866.1:c.*1017C= ENSP00000513993.1:n.*1017C=
ENST00000698867.1:n.5478C=
ENST00000698868.1:c.1368C= ENSP00000513994.1:p.Gly456=
ENST00000698869.1:c.1311+301C= ENSP00000513995.1:n.1311+301C=
ENST00000698870.1:c.1503C= ENSP00000513996.1:p.Gly501=
ENST00000698871.1:n.2026C=
ENST00000698872.1:c.*292C= ENSP00000513997.1:n.*292C=
ENST00000698873.1:c.*698C= ENSP00000513998.1:n.*698C=
ENST00000698874.1:c.963C= ENSP00000513999.1:p.Gly321=
ENST00000698875.1:n.1363C=
ENST00000698876.1:n.1551C=
ENST00000698877.1:n.1071C=
ENST00000698878.1:c.1497C= ENSP00000514000.1:p.Gly499=
ENST00000698880.1:c.1371C=
ENST00000345728.10:c.1503C= MANE Select ENSP00000339950.5:p.Gly501=
ENST00000279227.9:c.1515C= ENSP00000279227.5:p.Gly505=
ENST00000345728.9:c.1503C= ENSP00000339950.5:p.Gly501=
ENST00000545896.1:c.191C= ENSP00000440209.1:p.Ala64=
NM_031471.5:c.1503C= NP_113659.3:p.Gly501=
NM_178443.2:c.1515C= , LRG_180t1:c.1515C= NP_848537.1:p.Gly505=
XM_011545294.1:c.1515C= XP_011543596.1:p.Gly505=
XM_011545295.1:c.975C= XP_011543597.1:p.Gly325=
XM_011545296.1:c.975C= XP_011543598.1:p.Gly325=
XM_011545294.3:c.1515C= XP_011543596.1:p.Gly505=
XM_011545295.2:c.975C= XP_011543597.1:p.Gly325=
XM_017018398.2:c.1503C= XP_016873887.1:p.Gly501=
XM_017018399.1:c.963C= XP_016873888.1:p.Gly321=
NM_031471.6:c.1503C= MANE Select NP_113659.3:p.Gly501=
NM_001382361.1:c.1503C= NP_001369290.1:p.Gly501=
NM_001382362.1:c.1515C= NP_001369291.1:p.Gly505=
NM_001382363.1:c.963C= NP_001369292.1:p.Gly321=
NM_001382364.1:c.975C= NP_001369293.1:p.Gly325=
NM_001382448.1:c.1503C= NP_001369377.1:p.Gly501=
NM_178443.3:c.1515C= NP_848537.1:p.Gly505=