Canonical Allele Identifier: CA475151833

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990631C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223159C>T , CM000673.2:g.64223159C>T	GRCh38
NC_000011.9:g.63990631C>T , CM000673.1:g.63990631C>T	GRCh37
NC_000011.8:g.63747207C>T	NCBI36
NG_016360.1:g.21480C>T , LRG_180:g.21480C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1794C>T	ENSP00000279227.5:p.Arg598=
ENST00000540554.2:n.3306C>T
ENST00000541252.2:c.1242C>T	ENSP00000438885.2:p.Arg414=
ENST00000544997.6:c.1782C>T	ENSP00000445778.2:p.Arg594=
ENST00000545896.2:c.346C>T	ENSP00000440209.2:p.Pro116Ser
ENST00000546255.2:n.2086C>T
ENST00000698845.1:c.*977C>T	ENSP00000513981.1:n.*977C>T
ENST00000698846.1:n.2028C>T
ENST00000698847.1:c.*1187C>T	ENSP00000513982.1:n.*1187C>T
ENST00000698850.1:n.3803C>T
ENST00000698852.1:c.1782C>T	ENSP00000513984.1:p.Arg594=
ENST00000698853.1:c.*1011C>T	ENSP00000513985.1:n.*1011C>T
ENST00000698854.1:c.*1112C>T	ENSP00000513986.1:n.*1112C>T
ENST00000698855.1:n.3434C>T
ENST00000698856.1:n.3128C>T
ENST00000698859.1:n.2292C>T
ENST00000698860.1:c.1794C>T	ENSP00000513988.1:p.Arg598=
ENST00000698861.1:c.1782C>T	ENSP00000513989.1:p.Arg594=
ENST00000698862.1:c.*1078C>T	ENSP00000513990.1:n.*1078C>T
ENST00000698863.1:c.1782C>T	ENSP00000513991.1:p.Arg594=
ENST00000698864.1:n.2343C>T
ENST00000698865.1:c.1803C>T	ENSP00000513992.1:p.Arg601=
ENST00000698866.1:c.*1570C>T	ENSP00000513993.1:n.*1570C>T
ENST00000698867.1:n.5757C>T
ENST00000698868.1:c.1647C>T	ENSP00000513994.1:p.Arg549=
ENST00000698869.1:c.1548C>T	ENSP00000513995.1:p.Arg516=
ENST00000698870.1:c.1782C>T	ENSP00000513996.1:p.Arg594=
ENST00000698871.1:n.2305C>T
ENST00000698872.1:c.*571C>T	ENSP00000513997.1:n.*571C>T
ENST00000698873.1:c.*977C>T	ENSP00000513998.1:n.*977C>T
ENST00000698874.1:c.1242C>T	ENSP00000513999.1:p.Arg414=
ENST00000698875.1:n.1642C>T
ENST00000698876.1:n.1830C>T
ENST00000698877.1:n.1350C>T
ENST00000698878.1:c.1776C>T	ENSP00000514000.1:p.Arg592=
ENST00000698880.1:c.1650C>T
ENST00000345728.10:c.1782C>T MANE Select	ENSP00000339950.5:p.Arg594=
ENST00000279227.9:c.1794C>T	ENSP00000279227.5:p.Arg598=
ENST00000345728.9:c.1782C>T	ENSP00000339950.5:p.Arg594=
ENST00000545896.1:c.345C>T	ENSP00000440209.1:p.Arg115=
NM_031471.5:c.1782C>T	NP_113659.3:p.Arg594=
NM_178443.2:c.1794C>T , LRG_180t1:c.1794C>T	NP_848537.1:p.Arg598=
XM_011545294.1:c.1794C>T	XP_011543596.1:p.Arg598=
XM_011545295.1:c.1254C>T	XP_011543597.1:p.Arg418=
XM_011545296.1:c.1254C>T	XP_011543598.1:p.Arg418=
XM_011545294.3:c.1794C>T	XP_011543596.1:p.Arg598=
XM_011545295.2:c.1254C>T	XP_011543597.1:p.Arg418=
XM_017018398.2:c.1782C>T	XP_016873887.1:p.Arg594=
XM_017018399.1:c.1242C>T	XP_016873888.1:p.Arg414=
NM_031471.6:c.1782C>T MANE Select	NP_113659.3:p.Arg594=
NM_001382361.1:c.1782C>T	NP_001369290.1:p.Arg594=
NM_001382362.1:c.1794C>T	NP_001369291.1:p.Arg598=
NM_001382363.1:c.1242C>T	NP_001369292.1:p.Arg414=
NM_001382364.1:c.1254C>T	NP_001369293.1:p.Arg418=
NM_001382448.1:c.1782C>T	NP_001369377.1:p.Arg594=
NM_178443.3:c.1794C>T	NP_848537.1:p.Arg598=