Canonical Allele Identifier: CA1978638973
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220515G= , CM000673.2:g.64220515G= GRCh38
NC_000011.9:g.63987987G= , CM000673.1:g.63987987G= GRCh37
NC_000011.8:g.63744563G= NCBI36
NG_016360.1:g.18836G= , LRG_180:g.18836G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1403G= ENSP00000279227.5:p.Ser468=
ENST00000540554.2:n.2569G=
ENST00000541252.2:c.851G= ENSP00000438885.2:p.Ser284=
ENST00000541326.6:n.812G=
ENST00000544997.6:c.1391G= ENSP00000445778.2:p.Ser464=
ENST00000545896.2:c.80G= ENSP00000440209.2:p.Ser27=
ENST00000546255.2:n.1695G=
ENST00000698845.1:c.*586G= ENSP00000513981.1:n.*586G=
ENST00000698846.1:n.1637G=
ENST00000698847.1:c.*796G= ENSP00000513982.1:n.*796G=
ENST00000698849.1:n.511G=
ENST00000698850.1:n.1159G=
ENST00000698852.1:c.1391G= ENSP00000513984.1:p.Ser464=
ENST00000698853.1:c.*620G= ENSP00000513985.1:n.*620G=
ENST00000698854.1:c.*721G= ENSP00000513986.1:n.*721G=
ENST00000698855.1:n.3043G=
ENST00000698856.1:n.2737G=
ENST00000698859.1:n.1555G=
ENST00000698860.1:c.1403G= ENSP00000513988.1:p.Ser468=
ENST00000698861.1:c.1391G= ENSP00000513989.1:p.Ser464=
ENST00000698862.1:c.*687G= ENSP00000513990.1:n.*687G=
ENST00000698863.1:c.1391G= ENSP00000513991.1:p.Ser464=
ENST00000698864.1:n.1606G=
ENST00000698865.1:c.1412G= ENSP00000513992.1:p.Ser471=
ENST00000698866.1:c.*905G= ENSP00000513993.1:n.*905G=
ENST00000698867.1:n.5366G=
ENST00000698868.1:c.1256G= ENSP00000513994.1:p.Ser419=
ENST00000698869.1:c.1311+189G= ENSP00000513995.1:n.1311+189G=
ENST00000698870.1:c.1391G= ENSP00000513996.1:p.Ser464=
ENST00000698871.1:n.1914G=
ENST00000698872.1:c.*180G= ENSP00000513997.1:n.*180G=
ENST00000698873.1:c.*586G= ENSP00000513998.1:n.*586G=
ENST00000698874.1:c.851G= ENSP00000513999.1:p.Ser284=
ENST00000698875.1:n.1251G=
ENST00000698876.1:n.1439G=
ENST00000698877.1:n.959G=
ENST00000698878.1:c.1385G= ENSP00000514000.1:p.Ser462=
ENST00000698880.1:c.1259G=
ENST00000345728.10:c.1391G= MANE Select ENSP00000339950.5:p.Ser464=
ENST00000279227.9:c.1403G= ENSP00000279227.5:p.Ser468=
ENST00000345728.9:c.1391G= ENSP00000339950.5:p.Ser464=
ENST00000541326.5:n.807G=
ENST00000545896.1:c.79G= ENSP00000440209.1:p.Ala27=
NM_031471.5:c.1391G= NP_113659.3:p.Ser464=
NM_178443.2:c.1403G= , LRG_180t1:c.1403G= NP_848537.1:p.Ser468=
XM_011545294.1:c.1403G= XP_011543596.1:p.Ser468=
XM_011545295.1:c.863G= XP_011543597.1:p.Ser288=
XM_011545296.1:c.863G= XP_011543598.1:p.Ser288=
XM_011545294.3:c.1403G= XP_011543596.1:p.Ser468=
XM_011545295.2:c.863G= XP_011543597.1:p.Ser288=
XM_017018398.2:c.1391G= XP_016873887.1:p.Ser464=
XM_017018399.1:c.851G= XP_016873888.1:p.Ser284=
NM_031471.6:c.1391G= MANE Select NP_113659.3:p.Ser464=
NM_001382361.1:c.1391G= NP_001369290.1:p.Ser464=
NM_001382362.1:c.1403G= NP_001369291.1:p.Ser468=
NM_001382363.1:c.851G= NP_001369292.1:p.Ser284=
NM_001382364.1:c.863G= NP_001369293.1:p.Ser288=
NM_001382448.1:c.1391G= NP_001369377.1:p.Ser464=
NM_178443.3:c.1403G= NP_848537.1:p.Ser468=