Canonical Allele Identifier: CA1978639127

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220574G= , CM000673.2:g.64220574G=	GRCh38
NC_000011.9:g.63988046G= , CM000673.1:g.63988046G=	GRCh37
NC_000011.8:g.63744622G=	NCBI36
NG_016360.1:g.18895G= , LRG_180:g.18895G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1462G=	ENSP00000279227.5:p.Gly488=
ENST00000540554.2:n.2628G=
ENST00000541252.2:c.910G=	ENSP00000438885.2:p.Gly304=
ENST00000541326.6:n.871G=
ENST00000544997.6:c.1450G=	ENSP00000445778.2:p.Gly484=
ENST00000545896.2:c.139G=	ENSP00000440209.2:p.Gly47=
ENST00000546255.2:n.1754G=
ENST00000698845.1:c.*645G=	ENSP00000513981.1:n.*645G=
ENST00000698846.1:n.1696G=
ENST00000698847.1:c.*855G=	ENSP00000513982.1:n.*855G=
ENST00000698849.1:n.570G=
ENST00000698850.1:n.1218G=
ENST00000698852.1:c.1450G=	ENSP00000513984.1:p.Gly484=
ENST00000698853.1:c.*679G=	ENSP00000513985.1:n.*679G=
ENST00000698854.1:c.*780G=	ENSP00000513986.1:n.*780G=
ENST00000698855.1:n.3102G=
ENST00000698856.1:n.2796G=
ENST00000698859.1:n.1614G=
ENST00000698860.1:c.1462G=	ENSP00000513988.1:p.Gly488=
ENST00000698861.1:c.1450G=	ENSP00000513989.1:p.Gly484=
ENST00000698862.1:c.*746G=	ENSP00000513990.1:n.*746G=
ENST00000698863.1:c.1450G=	ENSP00000513991.1:p.Gly484=
ENST00000698864.1:n.1665G=
ENST00000698865.1:c.1471G=	ENSP00000513992.1:p.Gly491=
ENST00000698866.1:c.*964G=	ENSP00000513993.1:n.*964G=
ENST00000698867.1:n.5425G=
ENST00000698868.1:c.1315G=	ENSP00000513994.1:p.Gly439=
ENST00000698869.1:c.1311+248G=	ENSP00000513995.1:n.1311+248G=
ENST00000698870.1:c.1450G=	ENSP00000513996.1:p.Gly484=
ENST00000698871.1:n.1973G=
ENST00000698872.1:c.*239G=	ENSP00000513997.1:n.*239G=
ENST00000698873.1:c.*645G=	ENSP00000513998.1:n.*645G=
ENST00000698874.1:c.910G=	ENSP00000513999.1:p.Gly304=
ENST00000698875.1:n.1310G=
ENST00000698876.1:n.1498G=
ENST00000698877.1:n.1018G=
ENST00000698878.1:c.1444G=	ENSP00000514000.1:p.Gly482=
ENST00000698880.1:c.1318G=
ENST00000345728.10:c.1450G= MANE Select	ENSP00000339950.5:p.Gly484=
ENST00000279227.9:c.1462G=	ENSP00000279227.5:p.Gly488=
ENST00000345728.9:c.1450G=	ENSP00000339950.5:p.Gly484=
ENST00000541326.5:n.866G=
ENST00000545896.1:c.138G=	ENSP00000440209.1:p.Arg46=
NM_031471.5:c.1450G=	NP_113659.3:p.Gly484=
NM_178443.2:c.1462G= , LRG_180t1:c.1462G=	NP_848537.1:p.Gly488=
XM_011545294.1:c.1462G=	XP_011543596.1:p.Gly488=
XM_011545295.1:c.922G=	XP_011543597.1:p.Gly308=
XM_011545296.1:c.922G=	XP_011543598.1:p.Gly308=
XM_011545294.3:c.1462G=	XP_011543596.1:p.Gly488=
XM_011545295.2:c.922G=	XP_011543597.1:p.Gly308=
XM_017018398.2:c.1450G=	XP_016873887.1:p.Gly484=
XM_017018399.1:c.910G=	XP_016873888.1:p.Gly304=
NM_031471.6:c.1450G= MANE Select	NP_113659.3:p.Gly484=
NM_001382361.1:c.1450G=	NP_001369290.1:p.Gly484=
NM_001382362.1:c.1462G=	NP_001369291.1:p.Gly488=
NM_001382363.1:c.910G=	NP_001369292.1:p.Gly304=
NM_001382364.1:c.922G=	NP_001369293.1:p.Gly308=
NM_001382448.1:c.1450G=	NP_001369377.1:p.Gly484=
NM_178443.3:c.1462G=	NP_848537.1:p.Gly488=