Canonical Allele Identifier: CA1978639249

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220644T= , CM000673.2:g.64220644T=	GRCh38
NC_000011.9:g.63988116T= , CM000673.1:g.63988116T=	GRCh37
NC_000011.8:g.63744692T=	NCBI36
NG_016360.1:g.18965T= , LRG_180:g.18965T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1532T=	ENSP00000279227.5:p.Phe511=
ENST00000540554.2:n.2698T=
ENST00000541252.2:c.980T=	ENSP00000438885.2:p.Phe327=
ENST00000541326.6:n.941T=
ENST00000544997.6:c.1520T=	ENSP00000445778.2:p.Phe507=
ENST00000545896.2:c.209T=	ENSP00000440209.2:p.Phe70=
ENST00000546255.2:n.1824T=
ENST00000698845.1:c.*715T=	ENSP00000513981.1:n.*715T=
ENST00000698846.1:n.1766T=
ENST00000698847.1:c.*925T=	ENSP00000513982.1:n.*925T=
ENST00000698849.1:n.640T=
ENST00000698850.1:n.1288T=
ENST00000698852.1:c.1520T=	ENSP00000513984.1:p.Phe507=
ENST00000698853.1:c.*749T=	ENSP00000513985.1:n.*749T=
ENST00000698854.1:c.*850T=	ENSP00000513986.1:n.*850T=
ENST00000698855.1:n.3172T=
ENST00000698856.1:n.2866T=
ENST00000698859.1:n.1684T=
ENST00000698860.1:c.1532T=	ENSP00000513988.1:p.Phe511=
ENST00000698861.1:c.1520T=	ENSP00000513989.1:p.Phe507=
ENST00000698862.1:c.*816T=	ENSP00000513990.1:n.*816T=
ENST00000698863.1:c.1520T=	ENSP00000513991.1:p.Phe507=
ENST00000698864.1:n.1735T=
ENST00000698865.1:c.1541T=	ENSP00000513992.1:p.Phe514=
ENST00000698866.1:c.*1034T=	ENSP00000513993.1:n.*1034T=
ENST00000698867.1:n.5495T=
ENST00000698868.1:c.1385T=	ENSP00000513994.1:p.Phe462=
ENST00000698869.1:c.1311+318T=	ENSP00000513995.1:n.1311+318T=
ENST00000698870.1:c.1520T=	ENSP00000513996.1:p.Phe507=
ENST00000698871.1:n.2043T=
ENST00000698872.1:c.*309T=	ENSP00000513997.1:n.*309T=
ENST00000698873.1:c.*715T=	ENSP00000513998.1:n.*715T=
ENST00000698874.1:c.980T=	ENSP00000513999.1:p.Phe327=
ENST00000698875.1:n.1380T=
ENST00000698876.1:n.1568T=
ENST00000698877.1:n.1088T=
ENST00000698878.1:c.1514T=	ENSP00000514000.1:p.Phe505=
ENST00000698880.1:c.1388T=
ENST00000345728.10:c.1520T= MANE Select	ENSP00000339950.5:p.Phe507=
ENST00000279227.9:c.1532T=	ENSP00000279227.5:p.Phe511=
ENST00000345728.9:c.1520T=	ENSP00000339950.5:p.Phe507=
ENST00000545896.1:c.208T=	ENSP00000440209.1:p.Ser70=
NM_031471.5:c.1520T=	NP_113659.3:p.Phe507=
NM_178443.2:c.1532T= , LRG_180t1:c.1532T=	NP_848537.1:p.Phe511=
XM_011545294.1:c.1532T=	XP_011543596.1:p.Phe511=
XM_011545295.1:c.992T=	XP_011543597.1:p.Phe331=
XM_011545296.1:c.992T=	XP_011543598.1:p.Phe331=
XM_011545294.3:c.1532T=	XP_011543596.1:p.Phe511=
XM_011545295.2:c.992T=	XP_011543597.1:p.Phe331=
XM_017018398.2:c.1520T=	XP_016873887.1:p.Phe507=
XM_017018399.1:c.980T=	XP_016873888.1:p.Phe327=
NM_031471.6:c.1520T= MANE Select	NP_113659.3:p.Phe507=
NM_001382361.1:c.1520T=	NP_001369290.1:p.Phe507=
NM_001382362.1:c.1532T=	NP_001369291.1:p.Phe511=
NM_001382363.1:c.980T=	NP_001369292.1:p.Phe327=
NM_001382364.1:c.992T=	NP_001369293.1:p.Phe331=
NM_001382448.1:c.1520T=	NP_001369377.1:p.Phe507=
NM_178443.3:c.1532T=	NP_848537.1:p.Phe511=