Canonical Allele Identifier: CA475151797

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990569C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223097C>T , CM000673.2:g.64223097C>T	GRCh38
NC_000011.9:g.63990569C>T , CM000673.1:g.63990569C>T	GRCh37
NC_000011.8:g.63747145C>T	NCBI36
NG_016360.1:g.21418C>T , LRG_180:g.21418C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1732C>T	ENSP00000279227.5:p.Leu578=
ENST00000540554.2:n.3244C>T
ENST00000541252.2:c.1180C>T	ENSP00000438885.2:p.Leu394=
ENST00000544997.6:c.1720C>T	ENSP00000445778.2:p.Leu574=
ENST00000545896.2:c.284C>T	ENSP00000440209.2:p.Thr95Ile
ENST00000546255.2:n.2024C>T
ENST00000698845.1:c.*915C>T	ENSP00000513981.1:n.*915C>T
ENST00000698846.1:n.1966C>T
ENST00000698847.1:c.*1125C>T	ENSP00000513982.1:n.*1125C>T
ENST00000698850.1:n.3741C>T
ENST00000698852.1:c.1720C>T	ENSP00000513984.1:p.Leu574=
ENST00000698853.1:c.*949C>T	ENSP00000513985.1:n.*949C>T
ENST00000698854.1:c.*1050C>T	ENSP00000513986.1:n.*1050C>T
ENST00000698855.1:n.3372C>T
ENST00000698856.1:n.3066C>T
ENST00000698859.1:n.2230C>T
ENST00000698860.1:c.1732C>T	ENSP00000513988.1:p.Leu578=
ENST00000698861.1:c.1720C>T	ENSP00000513989.1:p.Leu574=
ENST00000698862.1:c.*1016C>T	ENSP00000513990.1:n.*1016C>T
ENST00000698863.1:c.1720C>T	ENSP00000513991.1:p.Leu574=
ENST00000698864.1:n.2281C>T
ENST00000698865.1:c.1741C>T	ENSP00000513992.1:p.Leu581=
ENST00000698866.1:c.*1508C>T	ENSP00000513993.1:n.*1508C>T
ENST00000698867.1:n.5695C>T
ENST00000698868.1:c.1585C>T	ENSP00000513994.1:p.Leu529=
ENST00000698869.1:c.1486C>T	ENSP00000513995.1:p.Leu496=
ENST00000698870.1:c.1720C>T	ENSP00000513996.1:p.Leu574=
ENST00000698871.1:n.2243C>T
ENST00000698872.1:c.*509C>T	ENSP00000513997.1:n.*509C>T
ENST00000698873.1:c.*915C>T	ENSP00000513998.1:n.*915C>T
ENST00000698874.1:c.1180C>T	ENSP00000513999.1:p.Leu394=
ENST00000698875.1:n.1580C>T
ENST00000698876.1:n.1768C>T
ENST00000698877.1:n.1288C>T
ENST00000698878.1:c.1714C>T	ENSP00000514000.1:p.Leu572=
ENST00000698880.1:c.1588C>T
ENST00000345728.10:c.1720C>T MANE Select	ENSP00000339950.5:p.Leu574=
ENST00000279227.9:c.1732C>T	ENSP00000279227.5:p.Leu578=
ENST00000345728.9:c.1720C>T	ENSP00000339950.5:p.Leu574=
ENST00000540554.1:n.356C>T
ENST00000545896.1:c.283C>T	ENSP00000440209.1:p.Leu95=
NM_031471.5:c.1720C>T	NP_113659.3:p.Leu574=
NM_178443.2:c.1732C>T , LRG_180t1:c.1732C>T	NP_848537.1:p.Leu578=
XM_011545294.1:c.1732C>T	XP_011543596.1:p.Leu578=
XM_011545295.1:c.1192C>T	XP_011543597.1:p.Leu398=
XM_011545296.1:c.1192C>T	XP_011543598.1:p.Leu398=
XM_011545294.3:c.1732C>T	XP_011543596.1:p.Leu578=
XM_011545295.2:c.1192C>T	XP_011543597.1:p.Leu398=
XM_017018398.2:c.1720C>T	XP_016873887.1:p.Leu574=
XM_017018399.1:c.1180C>T	XP_016873888.1:p.Leu394=
NM_031471.6:c.1720C>T MANE Select	NP_113659.3:p.Leu574=
NM_001382361.1:c.1720C>T	NP_001369290.1:p.Leu574=
NM_001382362.1:c.1732C>T	NP_001369291.1:p.Leu578=
NM_001382363.1:c.1180C>T	NP_001369292.1:p.Leu394=
NM_001382364.1:c.1192C>T	NP_001369293.1:p.Leu398=
NM_001382448.1:c.1720C>T	NP_001369377.1:p.Leu574=
NM_178443.3:c.1732C>T	NP_848537.1:p.Leu578=