Canonical Allele Identifier: CA1978639219
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220630C= , CM000673.2:g.64220630C= GRCh38
NC_000011.9:g.63988102C= , CM000673.1:g.63988102C= GRCh37
NC_000011.8:g.63744678C= NCBI36
NG_016360.1:g.18951C= , LRG_180:g.18951C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1518C= ENSP00000279227.5:p.Leu506=
ENST00000540554.2:n.2684C=
ENST00000541252.2:c.966C= ENSP00000438885.2:p.Leu322=
ENST00000541326.6:n.927C=
ENST00000544997.6:c.1506C= ENSP00000445778.2:p.Leu502=
ENST00000545896.2:c.195C= ENSP00000440209.2:p.Leu65=
ENST00000546255.2:n.1810C=
ENST00000698845.1:c.*701C= ENSP00000513981.1:n.*701C=
ENST00000698846.1:n.1752C=
ENST00000698847.1:c.*911C= ENSP00000513982.1:n.*911C=
ENST00000698849.1:n.626C=
ENST00000698850.1:n.1274C=
ENST00000698852.1:c.1506C= ENSP00000513984.1:p.Leu502=
ENST00000698853.1:c.*735C= ENSP00000513985.1:n.*735C=
ENST00000698854.1:c.*836C= ENSP00000513986.1:n.*836C=
ENST00000698855.1:n.3158C=
ENST00000698856.1:n.2852C=
ENST00000698859.1:n.1670C=
ENST00000698860.1:c.1518C= ENSP00000513988.1:p.Leu506=
ENST00000698861.1:c.1506C= ENSP00000513989.1:p.Leu502=
ENST00000698862.1:c.*802C= ENSP00000513990.1:n.*802C=
ENST00000698863.1:c.1506C= ENSP00000513991.1:p.Leu502=
ENST00000698864.1:n.1721C=
ENST00000698865.1:c.1527C= ENSP00000513992.1:p.Leu509=
ENST00000698866.1:c.*1020C= ENSP00000513993.1:n.*1020C=
ENST00000698867.1:n.5481C=
ENST00000698868.1:c.1371C= ENSP00000513994.1:p.Leu457=
ENST00000698869.1:c.1311+304C= ENSP00000513995.1:n.1311+304C=
ENST00000698870.1:c.1506C= ENSP00000513996.1:p.Leu502=
ENST00000698871.1:n.2029C=
ENST00000698872.1:c.*295C= ENSP00000513997.1:n.*295C=
ENST00000698873.1:c.*701C= ENSP00000513998.1:n.*701C=
ENST00000698874.1:c.966C= ENSP00000513999.1:p.Leu322=
ENST00000698875.1:n.1366C=
ENST00000698876.1:n.1554C=
ENST00000698877.1:n.1074C=
ENST00000698878.1:c.1500C= ENSP00000514000.1:p.Leu500=
ENST00000698880.1:c.1374C=
ENST00000345728.10:c.1506C= MANE Select ENSP00000339950.5:p.Leu502=
ENST00000279227.9:c.1518C= ENSP00000279227.5:p.Leu506=
ENST00000345728.9:c.1506C= ENSP00000339950.5:p.Leu502=
ENST00000545896.1:c.194C= ENSP00000440209.1:p.Ser65=
NM_031471.5:c.1506C= NP_113659.3:p.Leu502=
NM_178443.2:c.1518C= , LRG_180t1:c.1518C= NP_848537.1:p.Leu506=
XM_011545294.1:c.1518C= XP_011543596.1:p.Leu506=
XM_011545295.1:c.978C= XP_011543597.1:p.Leu326=
XM_011545296.1:c.978C= XP_011543598.1:p.Leu326=
XM_011545294.3:c.1518C= XP_011543596.1:p.Leu506=
XM_011545295.2:c.978C= XP_011543597.1:p.Leu326=
XM_017018398.2:c.1506C= XP_016873887.1:p.Leu502=
XM_017018399.1:c.966C= XP_016873888.1:p.Leu322=
NM_031471.6:c.1506C= MANE Select NP_113659.3:p.Leu502=
NM_001382361.1:c.1506C= NP_001369290.1:p.Leu502=
NM_001382362.1:c.1518C= NP_001369291.1:p.Leu506=
NM_001382363.1:c.966C= NP_001369292.1:p.Leu322=
NM_001382364.1:c.978C= NP_001369293.1:p.Leu326=
NM_001382448.1:c.1506C= NP_001369377.1:p.Leu502=
NM_178443.3:c.1518C= NP_848537.1:p.Leu506=