Canonical Allele Identifier: CA1978639231
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220634G= , CM000673.2:g.64220634G= GRCh38
NC_000011.9:g.63988106G= , CM000673.1:g.63988106G= GRCh37
NC_000011.8:g.63744682G= NCBI36
NG_016360.1:g.18955G= , LRG_180:g.18955G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1522G= ENSP00000279227.5:p.Ala508=
ENST00000540554.2:n.2688G=
ENST00000541252.2:c.970G= ENSP00000438885.2:p.Ala324=
ENST00000541326.6:n.931G=
ENST00000544997.6:c.1510G= ENSP00000445778.2:p.Ala504=
ENST00000545896.2:c.199G= ENSP00000440209.2:p.Ala67=
ENST00000546255.2:n.1814G=
ENST00000698845.1:c.*705G= ENSP00000513981.1:n.*705G=
ENST00000698846.1:n.1756G=
ENST00000698847.1:c.*915G= ENSP00000513982.1:n.*915G=
ENST00000698849.1:n.630G=
ENST00000698850.1:n.1278G=
ENST00000698852.1:c.1510G= ENSP00000513984.1:p.Ala504=
ENST00000698853.1:c.*739G= ENSP00000513985.1:n.*739G=
ENST00000698854.1:c.*840G= ENSP00000513986.1:n.*840G=
ENST00000698855.1:n.3162G=
ENST00000698856.1:n.2856G=
ENST00000698859.1:n.1674G=
ENST00000698860.1:c.1522G= ENSP00000513988.1:p.Ala508=
ENST00000698861.1:c.1510G= ENSP00000513989.1:p.Ala504=
ENST00000698862.1:c.*806G= ENSP00000513990.1:n.*806G=
ENST00000698863.1:c.1510G= ENSP00000513991.1:p.Ala504=
ENST00000698864.1:n.1725G=
ENST00000698865.1:c.1531G= ENSP00000513992.1:p.Ala511=
ENST00000698866.1:c.*1024G= ENSP00000513993.1:n.*1024G=
ENST00000698867.1:n.5485G=
ENST00000698868.1:c.1375G= ENSP00000513994.1:p.Ala459=
ENST00000698869.1:c.1311+308G= ENSP00000513995.1:n.1311+308G=
ENST00000698870.1:c.1510G= ENSP00000513996.1:p.Ala504=
ENST00000698871.1:n.2033G=
ENST00000698872.1:c.*299G= ENSP00000513997.1:n.*299G=
ENST00000698873.1:c.*705G= ENSP00000513998.1:n.*705G=
ENST00000698874.1:c.970G= ENSP00000513999.1:p.Ala324=
ENST00000698875.1:n.1370G=
ENST00000698876.1:n.1558G=
ENST00000698877.1:n.1078G=
ENST00000698878.1:c.1504G= ENSP00000514000.1:p.Ala502=
ENST00000698880.1:c.1378G=
ENST00000345728.10:c.1510G= MANE Select ENSP00000339950.5:p.Ala504=
ENST00000279227.9:c.1522G= ENSP00000279227.5:p.Ala508=
ENST00000345728.9:c.1510G= ENSP00000339950.5:p.Ala504=
ENST00000545896.1:c.198G= ENSP00000440209.1:p.Leu66=
NM_031471.5:c.1510G= NP_113659.3:p.Ala504=
NM_178443.2:c.1522G= , LRG_180t1:c.1522G= NP_848537.1:p.Ala508=
XM_011545294.1:c.1522G= XP_011543596.1:p.Ala508=
XM_011545295.1:c.982G= XP_011543597.1:p.Ala328=
XM_011545296.1:c.982G= XP_011543598.1:p.Ala328=
XM_011545294.3:c.1522G= XP_011543596.1:p.Ala508=
XM_011545295.2:c.982G= XP_011543597.1:p.Ala328=
XM_017018398.2:c.1510G= XP_016873887.1:p.Ala504=
XM_017018399.1:c.970G= XP_016873888.1:p.Ala324=
NM_031471.6:c.1510G= MANE Select NP_113659.3:p.Ala504=
NM_001382361.1:c.1510G= NP_001369290.1:p.Ala504=
NM_001382362.1:c.1522G= NP_001369291.1:p.Ala508=
NM_001382363.1:c.970G= NP_001369292.1:p.Ala324=
NM_001382364.1:c.982G= NP_001369293.1:p.Ala328=
NM_001382448.1:c.1510G= NP_001369377.1:p.Ala504=
NM_178443.3:c.1522G= NP_848537.1:p.Ala508=