Canonical Allele Identifier: CA1978642949

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223142C= , CM000673.2:g.64223142C=	GRCh38
NC_000011.9:g.63990614C= , CM000673.1:g.63990614C=	GRCh37
NC_000011.8:g.63747190C=	NCBI36
NG_016360.1:g.21463C= , LRG_180:g.21463C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1777C=	ENSP00000279227.5:p.Arg593=
ENST00000540554.2:n.3289C=
ENST00000541252.2:c.1225C=	ENSP00000438885.2:p.Arg409=
ENST00000544997.6:c.1765C=	ENSP00000445778.2:p.Arg589=
ENST00000545896.2:c.329C=	ENSP00000440209.2:p.Ala110=
ENST00000546255.2:n.2069C=
ENST00000698845.1:c.*960C=	ENSP00000513981.1:n.*960C=
ENST00000698846.1:n.2011C=
ENST00000698847.1:c.*1170C=	ENSP00000513982.1:n.*1170C=
ENST00000698850.1:n.3786C=
ENST00000698852.1:c.1765C=	ENSP00000513984.1:p.Arg589=
ENST00000698853.1:c.*994C=	ENSP00000513985.1:n.*994C=
ENST00000698854.1:c.*1095C=	ENSP00000513986.1:n.*1095C=
ENST00000698855.1:n.3417C=
ENST00000698856.1:n.3111C=
ENST00000698859.1:n.2275C=
ENST00000698860.1:c.1777C=	ENSP00000513988.1:p.Arg593=
ENST00000698861.1:c.1765C=	ENSP00000513989.1:p.Arg589=
ENST00000698862.1:c.*1061C=	ENSP00000513990.1:n.*1061C=
ENST00000698863.1:c.1765C=	ENSP00000513991.1:p.Arg589=
ENST00000698864.1:n.2326C=
ENST00000698865.1:c.1786C=	ENSP00000513992.1:p.Arg596=
ENST00000698866.1:c.*1553C=	ENSP00000513993.1:n.*1553C=
ENST00000698867.1:n.5740C=
ENST00000698868.1:c.1630C=	ENSP00000513994.1:p.Arg544=
ENST00000698869.1:c.1531C=	ENSP00000513995.1:p.Arg511=
ENST00000698870.1:c.1765C=	ENSP00000513996.1:p.Arg589=
ENST00000698871.1:n.2288C=
ENST00000698872.1:c.*554C=	ENSP00000513997.1:n.*554C=
ENST00000698873.1:c.*960C=	ENSP00000513998.1:n.*960C=
ENST00000698874.1:c.1225C=	ENSP00000513999.1:p.Arg409=
ENST00000698875.1:n.1625C=
ENST00000698876.1:n.1813C=
ENST00000698877.1:n.1333C=
ENST00000698878.1:c.1759C=	ENSP00000514000.1:p.Arg587=
ENST00000698880.1:c.1633C=
ENST00000345728.10:c.1765C= MANE Select	ENSP00000339950.5:p.Arg589=
ENST00000279227.9:c.1777C=	ENSP00000279227.5:p.Arg593=
ENST00000345728.9:c.1765C=	ENSP00000339950.5:p.Arg589=
ENST00000545896.1:c.328C=	ENSP00000440209.1:p.Arg110=
NM_031471.5:c.1765C=	NP_113659.3:p.Arg589=
NM_178443.2:c.1777C= , LRG_180t1:c.1777C=	NP_848537.1:p.Arg593=
XM_011545294.1:c.1777C=	XP_011543596.1:p.Arg593=
XM_011545295.1:c.1237C=	XP_011543597.1:p.Arg413=
XM_011545296.1:c.1237C=	XP_011543598.1:p.Arg413=
XM_011545294.3:c.1777C=	XP_011543596.1:p.Arg593=
XM_011545295.2:c.1237C=	XP_011543597.1:p.Arg413=
XM_017018398.2:c.1765C=	XP_016873887.1:p.Arg589=
XM_017018399.1:c.1225C=	XP_016873888.1:p.Arg409=
NM_031471.6:c.1765C= MANE Select	NP_113659.3:p.Arg589=
NM_001382361.1:c.1765C=	NP_001369290.1:p.Arg589=
NM_001382362.1:c.1777C=	NP_001369291.1:p.Arg593=
NM_001382363.1:c.1225C=	NP_001369292.1:p.Arg409=
NM_001382364.1:c.1237C=	NP_001369293.1:p.Arg413=
NM_001382448.1:c.1765C=	NP_001369377.1:p.Arg589=
NM_178443.3:c.1777C=	NP_848537.1:p.Arg593=