Canonical Allele Identifier: CA1978642790

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223081C= , CM000673.2:g.64223081C=	GRCh38
NC_000011.9:g.63990553C= , CM000673.1:g.63990553C=	GRCh37
NC_000011.8:g.63747129C=	NCBI36
NG_016360.1:g.21402C= , LRG_180:g.21402C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1716C=	ENSP00000279227.5:p.Gly572=
ENST00000540554.2:n.3228C=
ENST00000541252.2:c.1164C=	ENSP00000438885.2:p.Gly388=
ENST00000544997.6:c.1704C=	ENSP00000445778.2:p.Gly568=
ENST00000545896.2:c.268C=	ENSP00000440209.2:p.His90=
ENST00000546255.2:n.2008C=
ENST00000698845.1:c.*899C=	ENSP00000513981.1:n.*899C=
ENST00000698846.1:n.1950C=
ENST00000698847.1:c.*1109C=	ENSP00000513982.1:n.*1109C=
ENST00000698850.1:n.3725C=
ENST00000698852.1:c.1704C=	ENSP00000513984.1:p.Gly568=
ENST00000698853.1:c.*933C=	ENSP00000513985.1:n.*933C=
ENST00000698854.1:c.*1034C=	ENSP00000513986.1:n.*1034C=
ENST00000698855.1:n.3356C=
ENST00000698856.1:n.3050C=
ENST00000698859.1:n.2214C=
ENST00000698860.1:c.1716C=	ENSP00000513988.1:p.Gly572=
ENST00000698861.1:c.1704C=	ENSP00000513989.1:p.Gly568=
ENST00000698862.1:c.*1000C=	ENSP00000513990.1:n.*1000C=
ENST00000698863.1:c.1704C=	ENSP00000513991.1:p.Gly568=
ENST00000698864.1:n.2265C=
ENST00000698865.1:c.1725C=	ENSP00000513992.1:p.Gly575=
ENST00000698866.1:c.*1492C=	ENSP00000513993.1:n.*1492C=
ENST00000698867.1:n.5679C=
ENST00000698868.1:c.1569C=	ENSP00000513994.1:p.Gly523=
ENST00000698869.1:c.1470C=	ENSP00000513995.1:p.Gly490=
ENST00000698870.1:c.1704C=	ENSP00000513996.1:p.Gly568=
ENST00000698871.1:n.2227C=
ENST00000698872.1:c.*493C=	ENSP00000513997.1:n.*493C=
ENST00000698873.1:c.*899C=	ENSP00000513998.1:n.*899C=
ENST00000698874.1:c.1164C=	ENSP00000513999.1:p.Gly388=
ENST00000698875.1:n.1564C=
ENST00000698876.1:n.1752C=
ENST00000698877.1:n.1272C=
ENST00000698878.1:c.1698C=	ENSP00000514000.1:p.Gly566=
ENST00000698880.1:c.1572C=
ENST00000345728.10:c.1704C= MANE Select	ENSP00000339950.5:p.Gly568=
ENST00000279227.9:c.1716C=	ENSP00000279227.5:p.Gly572=
ENST00000345728.9:c.1704C=	ENSP00000339950.5:p.Gly568=
ENST00000540554.1:n.340C=
ENST00000545896.1:c.267C=	ENSP00000440209.1:p.Gly89=
NM_031471.5:c.1704C=	NP_113659.3:p.Gly568=
NM_178443.2:c.1716C= , LRG_180t1:c.1716C=	NP_848537.1:p.Gly572=
XM_011545294.1:c.1716C=	XP_011543596.1:p.Gly572=
XM_011545295.1:c.1176C=	XP_011543597.1:p.Gly392=
XM_011545296.1:c.1176C=	XP_011543598.1:p.Gly392=
XM_011545294.3:c.1716C=	XP_011543596.1:p.Gly572=
XM_011545295.2:c.1176C=	XP_011543597.1:p.Gly392=
XM_017018398.2:c.1704C=	XP_016873887.1:p.Gly568=
XM_017018399.1:c.1164C=	XP_016873888.1:p.Gly388=
NM_031471.6:c.1704C= MANE Select	NP_113659.3:p.Gly568=
NM_001382361.1:c.1704C=	NP_001369290.1:p.Gly568=
NM_001382362.1:c.1716C=	NP_001369291.1:p.Gly572=
NM_001382363.1:c.1164C=	NP_001369292.1:p.Gly388=
NM_001382364.1:c.1176C=	NP_001369293.1:p.Gly392=
NM_001382448.1:c.1704C=	NP_001369377.1:p.Gly568=
NM_178443.3:c.1716C=	NP_848537.1:p.Gly572=