Canonical Allele Identifier: CA381089421

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990527G>T (hg19) ; chr11:g.64223055G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223055G>T , CM000673.2:g.64223055G>T	GRCh38
NC_000011.9:g.63990527G>T , CM000673.1:g.63990527G>T	GRCh37
NC_000011.8:g.63747103G>T	NCBI36
NG_016360.1:g.21376G>T , LRG_180:g.21376G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1690G>T	ENSP00000279227.5:p.Gly564Cys
ENST00000540554.2:n.3202G>T
ENST00000541252.2:c.1138G>T	ENSP00000438885.2:p.Gly380Cys
ENST00000544997.6:c.1678G>T	ENSP00000445778.2:p.Gly560Cys
ENST00000545896.2:c.242G>T	ENSP00000440209.2:p.Gly81Val
ENST00000546255.2:n.1982G>T
ENST00000698845.1:c.*873G>T	ENSP00000513981.1:n.*873G>T
ENST00000698846.1:n.1924G>T
ENST00000698847.1:c.*1083G>T	ENSP00000513982.1:n.*1083G>T
ENST00000698850.1:n.3699G>T
ENST00000698852.1:c.1678G>T	ENSP00000513984.1:p.Gly560Cys
ENST00000698853.1:c.*907G>T	ENSP00000513985.1:n.*907G>T
ENST00000698854.1:c.*1008G>T	ENSP00000513986.1:n.*1008G>T
ENST00000698855.1:n.3330G>T
ENST00000698856.1:n.3024G>T
ENST00000698859.1:n.2188G>T
ENST00000698860.1:c.1690G>T	ENSP00000513988.1:p.Gly564Cys
ENST00000698861.1:c.1678G>T	ENSP00000513989.1:p.Gly560Cys
ENST00000698862.1:c.*974G>T	ENSP00000513990.1:n.*974G>T
ENST00000698863.1:c.1678G>T	ENSP00000513991.1:p.Gly560Cys
ENST00000698864.1:n.2239G>T
ENST00000698865.1:c.1699G>T	ENSP00000513992.1:p.Gly567Cys
ENST00000698866.1:c.*1466G>T	ENSP00000513993.1:n.*1466G>T
ENST00000698867.1:n.5653G>T
ENST00000698868.1:c.1543G>T	ENSP00000513994.1:p.Gly515Cys
ENST00000698869.1:c.1444G>T	ENSP00000513995.1:p.Gly482Cys
ENST00000698870.1:c.1678G>T	ENSP00000513996.1:p.Gly560Cys
ENST00000698871.1:n.2201G>T
ENST00000698872.1:c.*467G>T	ENSP00000513997.1:n.*467G>T
ENST00000698873.1:c.*873G>T	ENSP00000513998.1:n.*873G>T
ENST00000698874.1:c.1138G>T	ENSP00000513999.1:p.Gly380Cys
ENST00000698875.1:n.1538G>T
ENST00000698876.1:n.1726G>T
ENST00000698877.1:n.1246G>T
ENST00000698878.1:c.1672G>T	ENSP00000514000.1:p.Gly558Cys
ENST00000698880.1:c.1546G>T
ENST00000345728.10:c.1678G>T MANE Select	ENSP00000339950.5:p.Gly560Cys
ENST00000279227.9:c.1690G>T	ENSP00000279227.5:p.Gly564Cys
ENST00000345728.9:c.1678G>T	ENSP00000339950.5:p.Gly560Cys
ENST00000540554.1:n.314G>T
ENST00000545896.1:c.241G>T	ENSP00000440209.1:p.Gly81Cys
NM_031471.5:c.1678G>T	NP_113659.3:p.Gly560Cys
NM_178443.2:c.1690G>T , LRG_180t1:c.1690G>T	NP_848537.1:p.Gly564Cys
XM_011545294.1:c.1690G>T	XP_011543596.1:p.Gly564Cys
XM_011545295.1:c.1150G>T	XP_011543597.1:p.Gly384Cys
XM_011545296.1:c.1150G>T	XP_011543598.1:p.Gly384Cys
XM_011545294.3:c.1690G>T	XP_011543596.1:p.Gly564Cys
XM_011545295.2:c.1150G>T	XP_011543597.1:p.Gly384Cys
XM_017018398.2:c.1678G>T	XP_016873887.1:p.Gly560Cys
XM_017018399.1:c.1138G>T	XP_016873888.1:p.Gly380Cys
NM_031471.6:c.1678G>T MANE Select	NP_113659.3:p.Gly560Cys
NM_001382361.1:c.1678G>T	NP_001369290.1:p.Gly560Cys
NM_001382362.1:c.1690G>T	NP_001369291.1:p.Gly564Cys
NM_001382363.1:c.1138G>T	NP_001369292.1:p.Gly380Cys
NM_001382364.1:c.1150G>T	NP_001369293.1:p.Gly384Cys
NM_001382448.1:c.1678G>T	NP_001369377.1:p.Gly560Cys
NM_178443.3:c.1690G>T	NP_848537.1:p.Gly564Cys