Canonical Allele Identifier: CA381087931

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63988047G>T (hg19) ; chr11:g.64220575G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220575G>T , CM000673.2:g.64220575G>T	GRCh38
NC_000011.9:g.63988047G>T , CM000673.1:g.63988047G>T	GRCh37
NC_000011.8:g.63744623G>T	NCBI36
NG_016360.1:g.18896G>T , LRG_180:g.18896G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1463G>T	ENSP00000279227.5:p.Gly488Val
ENST00000540554.2:n.2629G>T
ENST00000541252.2:c.911G>T	ENSP00000438885.2:p.Gly304Val
ENST00000541326.6:n.872G>T
ENST00000544997.6:c.1451G>T	ENSP00000445778.2:p.Gly484Val
ENST00000545896.2:c.140G>T	ENSP00000440209.2:p.Gly47Val
ENST00000546255.2:n.1755G>T
ENST00000698845.1:c.*646G>T	ENSP00000513981.1:n.*646G>T
ENST00000698846.1:n.1697G>T
ENST00000698847.1:c.*856G>T	ENSP00000513982.1:n.*856G>T
ENST00000698849.1:n.571G>T
ENST00000698850.1:n.1219G>T
ENST00000698852.1:c.1451G>T	ENSP00000513984.1:p.Gly484Val
ENST00000698853.1:c.*680G>T	ENSP00000513985.1:n.*680G>T
ENST00000698854.1:c.*781G>T	ENSP00000513986.1:n.*781G>T
ENST00000698855.1:n.3103G>T
ENST00000698856.1:n.2797G>T
ENST00000698859.1:n.1615G>T
ENST00000698860.1:c.1463G>T	ENSP00000513988.1:p.Gly488Val
ENST00000698861.1:c.1451G>T	ENSP00000513989.1:p.Gly484Val
ENST00000698862.1:c.*747G>T	ENSP00000513990.1:n.*747G>T
ENST00000698863.1:c.1451G>T	ENSP00000513991.1:p.Gly484Val
ENST00000698864.1:n.1666G>T
ENST00000698865.1:c.1472G>T	ENSP00000513992.1:p.Gly491Val
ENST00000698866.1:c.*965G>T	ENSP00000513993.1:n.*965G>T
ENST00000698867.1:n.5426G>T
ENST00000698868.1:c.1316G>T	ENSP00000513994.1:p.Gly439Val
ENST00000698869.1:c.1311+249G>T	ENSP00000513995.1:n.1311+249G>T
ENST00000698870.1:c.1451G>T	ENSP00000513996.1:p.Gly484Val
ENST00000698871.1:n.1974G>T
ENST00000698872.1:c.*240G>T	ENSP00000513997.1:n.*240G>T
ENST00000698873.1:c.*646G>T	ENSP00000513998.1:n.*646G>T
ENST00000698874.1:c.911G>T	ENSP00000513999.1:p.Gly304Val
ENST00000698875.1:n.1311G>T
ENST00000698876.1:n.1499G>T
ENST00000698877.1:n.1019G>T
ENST00000698878.1:c.1445G>T	ENSP00000514000.1:p.Gly482Val
ENST00000698880.1:c.1319G>T
ENST00000345728.10:c.1451G>T MANE Select	ENSP00000339950.5:p.Gly484Val
ENST00000279227.9:c.1463G>T	ENSP00000279227.5:p.Gly488Val
ENST00000345728.9:c.1451G>T	ENSP00000339950.5:p.Gly484Val
ENST00000541326.5:n.867G>T
ENST00000545896.1:c.139G>T	ENSP00000440209.1:p.Ala47Ser
NM_031471.5:c.1451G>T	NP_113659.3:p.Gly484Val
NM_178443.2:c.1463G>T , LRG_180t1:c.1463G>T	NP_848537.1:p.Gly488Val
XM_011545294.1:c.1463G>T	XP_011543596.1:p.Gly488Val
XM_011545295.1:c.923G>T	XP_011543597.1:p.Gly308Val
XM_011545296.1:c.923G>T	XP_011543598.1:p.Gly308Val
XM_011545294.3:c.1463G>T	XP_011543596.1:p.Gly488Val
XM_011545295.2:c.923G>T	XP_011543597.1:p.Gly308Val
XM_017018398.2:c.1451G>T	XP_016873887.1:p.Gly484Val
XM_017018399.1:c.911G>T	XP_016873888.1:p.Gly304Val
NM_031471.6:c.1451G>T MANE Select	NP_113659.3:p.Gly484Val
NM_001382361.1:c.1451G>T	NP_001369290.1:p.Gly484Val
NM_001382362.1:c.1463G>T	NP_001369291.1:p.Gly488Val
NM_001382363.1:c.911G>T	NP_001369292.1:p.Gly304Val
NM_001382364.1:c.923G>T	NP_001369293.1:p.Gly308Val
NM_001382448.1:c.1451G>T	NP_001369377.1:p.Gly484Val
NM_178443.3:c.1463G>T	NP_848537.1:p.Gly488Val