Canonical Allele Identifier: CA475151801

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990574C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223102C>T , CM000673.2:g.64223102C>T	GRCh38
NC_000011.9:g.63990574C>T , CM000673.1:g.63990574C>T	GRCh37
NC_000011.8:g.63747150C>T	NCBI36
NG_016360.1:g.21423C>T , LRG_180:g.21423C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1737C>T	ENSP00000279227.5:p.Ile579=
ENST00000540554.2:n.3249C>T
ENST00000541252.2:c.1185C>T	ENSP00000438885.2:p.Ile395=
ENST00000544997.6:c.1725C>T	ENSP00000445778.2:p.Ile575=
ENST00000545896.2:c.289C>T	ENSP00000440209.2:p.Pro97Ser
ENST00000546255.2:n.2029C>T
ENST00000698845.1:c.*920C>T	ENSP00000513981.1:n.*920C>T
ENST00000698846.1:n.1971C>T
ENST00000698847.1:c.*1130C>T	ENSP00000513982.1:n.*1130C>T
ENST00000698850.1:n.3746C>T
ENST00000698852.1:c.1725C>T	ENSP00000513984.1:p.Ile575=
ENST00000698853.1:c.*954C>T	ENSP00000513985.1:n.*954C>T
ENST00000698854.1:c.*1055C>T	ENSP00000513986.1:n.*1055C>T
ENST00000698855.1:n.3377C>T
ENST00000698856.1:n.3071C>T
ENST00000698859.1:n.2235C>T
ENST00000698860.1:c.1737C>T	ENSP00000513988.1:p.Ile579=
ENST00000698861.1:c.1725C>T	ENSP00000513989.1:p.Ile575=
ENST00000698862.1:c.*1021C>T	ENSP00000513990.1:n.*1021C>T
ENST00000698863.1:c.1725C>T	ENSP00000513991.1:p.Ile575=
ENST00000698864.1:n.2286C>T
ENST00000698865.1:c.1746C>T	ENSP00000513992.1:p.Ile582=
ENST00000698866.1:c.*1513C>T	ENSP00000513993.1:n.*1513C>T
ENST00000698867.1:n.5700C>T
ENST00000698868.1:c.1590C>T	ENSP00000513994.1:p.Ile530=
ENST00000698869.1:c.1491C>T	ENSP00000513995.1:p.Ile497=
ENST00000698870.1:c.1725C>T	ENSP00000513996.1:p.Ile575=
ENST00000698871.1:n.2248C>T
ENST00000698872.1:c.*514C>T	ENSP00000513997.1:n.*514C>T
ENST00000698873.1:c.*920C>T	ENSP00000513998.1:n.*920C>T
ENST00000698874.1:c.1185C>T	ENSP00000513999.1:p.Ile395=
ENST00000698875.1:n.1585C>T
ENST00000698876.1:n.1773C>T
ENST00000698877.1:n.1293C>T
ENST00000698878.1:c.1719C>T	ENSP00000514000.1:p.Ile573=
ENST00000698880.1:c.1593C>T
ENST00000345728.10:c.1725C>T MANE Select	ENSP00000339950.5:p.Ile575=
ENST00000279227.9:c.1737C>T	ENSP00000279227.5:p.Ile579=
ENST00000345728.9:c.1725C>T	ENSP00000339950.5:p.Ile575=
ENST00000540554.1:n.361C>T
ENST00000545896.1:c.288C>T	ENSP00000440209.1:p.Ile96=
NM_031471.5:c.1725C>T	NP_113659.3:p.Ile575=
NM_178443.2:c.1737C>T , LRG_180t1:c.1737C>T	NP_848537.1:p.Ile579=
XM_011545294.1:c.1737C>T	XP_011543596.1:p.Ile579=
XM_011545295.1:c.1197C>T	XP_011543597.1:p.Ile399=
XM_011545296.1:c.1197C>T	XP_011543598.1:p.Ile399=
XM_011545294.3:c.1737C>T	XP_011543596.1:p.Ile579=
XM_011545295.2:c.1197C>T	XP_011543597.1:p.Ile399=
XM_017018398.2:c.1725C>T	XP_016873887.1:p.Ile575=
XM_017018399.1:c.1185C>T	XP_016873888.1:p.Ile395=
NM_031471.6:c.1725C>T MANE Select	NP_113659.3:p.Ile575=
NM_001382361.1:c.1725C>T	NP_001369290.1:p.Ile575=
NM_001382362.1:c.1737C>T	NP_001369291.1:p.Ile579=
NM_001382363.1:c.1185C>T	NP_001369292.1:p.Ile395=
NM_001382364.1:c.1197C>T	NP_001369293.1:p.Ile399=
NM_001382448.1:c.1725C>T	NP_001369377.1:p.Ile575=
NM_178443.3:c.1737C>T	NP_848537.1:p.Ile579=