Canonical Allele Identifier: CA381087453

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987937C>G (hg19) ; chr11:g.64220465C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220465C>G , CM000673.2:g.64220465C>G	GRCh38
NC_000011.9:g.63987937C>G , CM000673.1:g.63987937C>G	GRCh37
NC_000011.8:g.63744513C>G	NCBI36
NG_016360.1:g.18786C>G , LRG_180:g.18786C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1353C>G	ENSP00000279227.5:p.Gly451=
ENST00000540554.2:n.2519C>G
ENST00000541252.2:c.801C>G	ENSP00000438885.2:p.Gly267=
ENST00000541326.6:n.762C>G
ENST00000544997.6:c.1341C>G	ENSP00000445778.2:p.Gly447=
ENST00000545896.2:c.30C>G	ENSP00000440209.2:p.Gly10=
ENST00000546255.2:n.1645C>G
ENST00000698845.1:c.*536C>G	ENSP00000513981.1:n.*536C>G
ENST00000698846.1:n.1587C>G
ENST00000698847.1:c.*746C>G	ENSP00000513982.1:n.*746C>G
ENST00000698848.1:n.639C>G
ENST00000698849.1:n.461C>G
ENST00000698850.1:n.1109C>G
ENST00000698852.1:c.1341C>G	ENSP00000513984.1:p.Gly447=
ENST00000698853.1:c.*570C>G	ENSP00000513985.1:n.*570C>G
ENST00000698854.1:c.*671C>G	ENSP00000513986.1:n.*671C>G
ENST00000698855.1:n.2993C>G
ENST00000698856.1:n.2687C>G
ENST00000698859.1:n.1505C>G
ENST00000698860.1:c.1353C>G	ENSP00000513988.1:p.Gly451=
ENST00000698861.1:c.1341C>G	ENSP00000513989.1:p.Gly447=
ENST00000698862.1:c.*637C>G	ENSP00000513990.1:n.*637C>G
ENST00000698863.1:c.1341C>G	ENSP00000513991.1:p.Gly447=
ENST00000698864.1:n.1556C>G
ENST00000698865.1:c.1362C>G	ENSP00000513992.1:p.Gly454=
ENST00000698866.1:c.*855C>G	ENSP00000513993.1:n.*855C>G
ENST00000698867.1:n.5316C>G
ENST00000698868.1:c.1206C>G	ENSP00000513994.1:p.Gly402=
ENST00000698869.1:c.1311+139C>G	ENSP00000513995.1:n.1311+139C>G
ENST00000698870.1:c.1341C>G	ENSP00000513996.1:p.Gly447=
ENST00000698871.1:n.1864C>G
ENST00000698872.1:c.*130C>G	ENSP00000513997.1:n.*130C>G
ENST00000698873.1:c.*536C>G	ENSP00000513998.1:n.*536C>G
ENST00000698874.1:c.801C>G	ENSP00000513999.1:p.Gly267=
ENST00000698875.1:n.1201C>G
ENST00000698876.1:n.1389C>G
ENST00000698877.1:n.909C>G
ENST00000698878.1:c.1335C>G	ENSP00000514000.1:p.Gly445=
ENST00000698880.1:c.1209C>G
ENST00000345728.10:c.1341C>G MANE Select	ENSP00000339950.5:p.Gly447=
ENST00000279227.9:c.1353C>G	ENSP00000279227.5:p.Gly451=
ENST00000345728.9:c.1341C>G	ENSP00000339950.5:p.Gly447=
ENST00000541326.5:n.757C>G
ENST00000545896.1:c.29C>G	ENSP00000440209.1:p.Ala10Gly
NM_031471.5:c.1341C>G	NP_113659.3:p.Gly447=
NM_178443.2:c.1353C>G , LRG_180t1:c.1353C>G	NP_848537.1:p.Gly451=
XM_011545294.1:c.1353C>G	XP_011543596.1:p.Gly451=
XM_011545295.1:c.813C>G	XP_011543597.1:p.Gly271=
XM_011545296.1:c.813C>G	XP_011543598.1:p.Gly271=
XM_011545294.3:c.1353C>G	XP_011543596.1:p.Gly451=
XM_011545295.2:c.813C>G	XP_011543597.1:p.Gly271=
XM_017018398.2:c.1341C>G	XP_016873887.1:p.Gly447=
XM_017018399.1:c.801C>G	XP_016873888.1:p.Gly267=
NM_031471.6:c.1341C>G MANE Select	NP_113659.3:p.Gly447=
NM_001382361.1:c.1341C>G	NP_001369290.1:p.Gly447=
NM_001382362.1:c.1353C>G	NP_001369291.1:p.Gly451=
NM_001382363.1:c.801C>G	NP_001369292.1:p.Gly267=
NM_001382364.1:c.813C>G	NP_001369293.1:p.Gly271=
NM_001382448.1:c.1341C>G	NP_001369377.1:p.Gly447=
NM_178443.3:c.1353C>G	NP_848537.1:p.Gly451=