Canonical Allele Identifier: CA475151725

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987726C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220254C>A , CM000673.2:g.64220254C>A	GRCh38
NC_000011.9:g.63987726C>A , CM000673.1:g.63987726C>A	GRCh37
NC_000011.8:g.63744302C>A	NCBI36
NG_016360.1:g.18575C>A , LRG_180:g.18575C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1251C>A	ENSP00000279227.5:p.Gly417=
ENST00000540554.2:n.2308C>A
ENST00000541252.2:c.699C>A	ENSP00000438885.2:p.Gly233=
ENST00000541326.6:n.551C>A
ENST00000544997.6:c.1239C>A	ENSP00000445778.2:p.Gly413=
ENST00000546255.2:n.1434C>A
ENST00000698845.1:c.*434C>A	ENSP00000513981.1:n.*434C>A
ENST00000698846.1:n.1376C>A
ENST00000698847.1:c.*644C>A	ENSP00000513982.1:n.*644C>A
ENST00000698848.1:n.428C>A
ENST00000698849.1:n.359C>A
ENST00000698850.1:n.898C>A
ENST00000698852.1:c.1239C>A	ENSP00000513984.1:p.Gly413=
ENST00000698853.1:c.*468C>A	ENSP00000513985.1:n.*468C>A
ENST00000698854.1:c.*569C>A	ENSP00000513986.1:n.*569C>A
ENST00000698855.1:n.2891C>A
ENST00000698856.1:n.2476C>A
ENST00000698859.1:n.1403C>A
ENST00000698860.1:c.1251C>A	ENSP00000513988.1:p.Gly417=
ENST00000698861.1:c.1239C>A	ENSP00000513989.1:p.Gly413=
ENST00000698862.1:c.*535C>A	ENSP00000513990.1:n.*535C>A
ENST00000698863.1:c.1239C>A	ENSP00000513991.1:p.Gly413=
ENST00000698864.1:n.1345C>A
ENST00000698865.1:c.1260C>A	ENSP00000513992.1:p.Gly420=
ENST00000698866.1:c.*644C>A	ENSP00000513993.1:n.*644C>A
ENST00000698867.1:n.5214C>A
ENST00000698868.1:c.1104C>A	ENSP00000513994.1:p.Gly368=
ENST00000698869.1:c.1239C>A	ENSP00000513995.1:p.Gly413=
ENST00000698870.1:c.1239C>A	ENSP00000513996.1:p.Gly413=
ENST00000698871.1:n.1762C>A
ENST00000698872.1:c.*28C>A	ENSP00000513997.1:n.*28C>A
ENST00000698873.1:c.*434C>A	ENSP00000513998.1:n.*434C>A
ENST00000698874.1:c.699C>A	ENSP00000513999.1:p.Gly233=
ENST00000698875.1:n.1099C>A
ENST00000698876.1:n.1178C>A
ENST00000698877.1:n.807C>A
ENST00000698878.1:c.1239C>A	ENSP00000514000.1:p.Gly413=
ENST00000698880.1:c.1079C>A
ENST00000345728.10:c.1239C>A MANE Select	ENSP00000339950.5:p.Gly413=
ENST00000279227.9:c.1251C>A	ENSP00000279227.5:p.Gly417=
ENST00000345728.9:c.1239C>A	ENSP00000339950.5:p.Gly413=
ENST00000540957.1:n.392C>A
ENST00000541326.5:n.546C>A
NM_031471.5:c.1239C>A	NP_113659.3:p.Gly413=
NM_178443.2:c.1251C>A , LRG_180t1:c.1251C>A	NP_848537.1:p.Gly417=
XM_011545294.1:c.1251C>A	XP_011543596.1:p.Gly417=
XM_011545295.1:c.711C>A	XP_011543597.1:p.Gly237=
XM_011545296.1:c.711C>A	XP_011543598.1:p.Gly237=
XM_011545294.3:c.1251C>A	XP_011543596.1:p.Gly417=
XM_011545295.2:c.711C>A	XP_011543597.1:p.Gly237=
XM_017018398.2:c.1239C>A	XP_016873887.1:p.Gly413=
XM_017018399.1:c.699C>A	XP_016873888.1:p.Gly233=
NM_031471.6:c.1239C>A MANE Select	NP_113659.3:p.Gly413=
NM_001382361.1:c.1239C>A	NP_001369290.1:p.Gly413=
NM_001382362.1:c.1251C>A	NP_001369291.1:p.Gly417=
NM_001382363.1:c.699C>A	NP_001369292.1:p.Gly233=
NM_001382364.1:c.711C>A	NP_001369293.1:p.Gly237=
NM_001382448.1:c.1239C>A	NP_001369377.1:p.Gly413=
NM_178443.3:c.1251C>A	NP_848537.1:p.Gly417=