Canonical Allele Identifier: CA475151821

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990604C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223132C>T , CM000673.2:g.64223132C>T	GRCh38
NC_000011.9:g.63990604C>T , CM000673.1:g.63990604C>T	GRCh37
NC_000011.8:g.63747180C>T	NCBI36
NG_016360.1:g.21453C>T , LRG_180:g.21453C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1767C>T	ENSP00000279227.5:p.Val589=
ENST00000540554.2:n.3279C>T
ENST00000541252.2:c.1215C>T	ENSP00000438885.2:p.Val405=
ENST00000544997.6:c.1755C>T	ENSP00000445778.2:p.Val585=
ENST00000545896.2:c.319C>T	ENSP00000440209.2:p.Gln107Ter
ENST00000546255.2:n.2059C>T
ENST00000698845.1:c.*950C>T	ENSP00000513981.1:n.*950C>T
ENST00000698846.1:n.2001C>T
ENST00000698847.1:c.*1160C>T	ENSP00000513982.1:n.*1160C>T
ENST00000698850.1:n.3776C>T
ENST00000698852.1:c.1755C>T	ENSP00000513984.1:p.Val585=
ENST00000698853.1:c.*984C>T	ENSP00000513985.1:n.*984C>T
ENST00000698854.1:c.*1085C>T	ENSP00000513986.1:n.*1085C>T
ENST00000698855.1:n.3407C>T
ENST00000698856.1:n.3101C>T
ENST00000698859.1:n.2265C>T
ENST00000698860.1:c.1767C>T	ENSP00000513988.1:p.Val589=
ENST00000698861.1:c.1755C>T	ENSP00000513989.1:p.Val585=
ENST00000698862.1:c.*1051C>T	ENSP00000513990.1:n.*1051C>T
ENST00000698863.1:c.1755C>T	ENSP00000513991.1:p.Val585=
ENST00000698864.1:n.2316C>T
ENST00000698865.1:c.1776C>T	ENSP00000513992.1:p.Val592=
ENST00000698866.1:c.*1543C>T	ENSP00000513993.1:n.*1543C>T
ENST00000698867.1:n.5730C>T
ENST00000698868.1:c.1620C>T	ENSP00000513994.1:p.Val540=
ENST00000698869.1:c.1521C>T	ENSP00000513995.1:p.Val507=
ENST00000698870.1:c.1755C>T	ENSP00000513996.1:p.Val585=
ENST00000698871.1:n.2278C>T
ENST00000698872.1:c.*544C>T	ENSP00000513997.1:n.*544C>T
ENST00000698873.1:c.*950C>T	ENSP00000513998.1:n.*950C>T
ENST00000698874.1:c.1215C>T	ENSP00000513999.1:p.Val405=
ENST00000698875.1:n.1615C>T
ENST00000698876.1:n.1803C>T
ENST00000698877.1:n.1323C>T
ENST00000698878.1:c.1749C>T	ENSP00000514000.1:p.Val583=
ENST00000698880.1:c.1623C>T
ENST00000345728.10:c.1755C>T MANE Select	ENSP00000339950.5:p.Val585=
ENST00000279227.9:c.1767C>T	ENSP00000279227.5:p.Val589=
ENST00000345728.9:c.1755C>T	ENSP00000339950.5:p.Val585=
ENST00000545896.1:c.318C>T	ENSP00000440209.1:p.Val106=
NM_031471.5:c.1755C>T	NP_113659.3:p.Val585=
NM_178443.2:c.1767C>T , LRG_180t1:c.1767C>T	NP_848537.1:p.Val589=
XM_011545294.1:c.1767C>T	XP_011543596.1:p.Val589=
XM_011545295.1:c.1227C>T	XP_011543597.1:p.Val409=
XM_011545296.1:c.1227C>T	XP_011543598.1:p.Val409=
XM_011545294.3:c.1767C>T	XP_011543596.1:p.Val589=
XM_011545295.2:c.1227C>T	XP_011543597.1:p.Val409=
XM_017018398.2:c.1755C>T	XP_016873887.1:p.Val585=
XM_017018399.1:c.1215C>T	XP_016873888.1:p.Val405=
NM_031471.6:c.1755C>T MANE Select	NP_113659.3:p.Val585=
NM_001382361.1:c.1755C>T	NP_001369290.1:p.Val585=
NM_001382362.1:c.1767C>T	NP_001369291.1:p.Val589=
NM_001382363.1:c.1215C>T	NP_001369292.1:p.Val405=
NM_001382364.1:c.1227C>T	NP_001369293.1:p.Val409=
NM_001382448.1:c.1755C>T	NP_001369377.1:p.Val585=
NM_178443.3:c.1767C>T	NP_848537.1:p.Val589=