Canonical Allele Identifier: CA475151757

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990529C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223057C>A , CM000673.2:g.64223057C>A	GRCh38
NC_000011.9:g.63990529C>A , CM000673.1:g.63990529C>A	GRCh37
NC_000011.8:g.63747105C>A	NCBI36
NG_016360.1:g.21378C>A , LRG_180:g.21378C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1692C>A	ENSP00000279227.5:p.Gly564=
ENST00000540554.2:n.3204C>A
ENST00000541252.2:c.1140C>A	ENSP00000438885.2:p.Gly380=
ENST00000544997.6:c.1680C>A	ENSP00000445778.2:p.Gly560=
ENST00000545896.2:c.244C>A	ENSP00000440209.2:p.Gln82Lys
ENST00000546255.2:n.1984C>A
ENST00000698845.1:c.*875C>A	ENSP00000513981.1:n.*875C>A
ENST00000698846.1:n.1926C>A
ENST00000698847.1:c.*1085C>A	ENSP00000513982.1:n.*1085C>A
ENST00000698850.1:n.3701C>A
ENST00000698852.1:c.1680C>A	ENSP00000513984.1:p.Gly560=
ENST00000698853.1:c.*909C>A	ENSP00000513985.1:n.*909C>A
ENST00000698854.1:c.*1010C>A	ENSP00000513986.1:n.*1010C>A
ENST00000698855.1:n.3332C>A
ENST00000698856.1:n.3026C>A
ENST00000698859.1:n.2190C>A
ENST00000698860.1:c.1692C>A	ENSP00000513988.1:p.Gly564=
ENST00000698861.1:c.1680C>A	ENSP00000513989.1:p.Gly560=
ENST00000698862.1:c.*976C>A	ENSP00000513990.1:n.*976C>A
ENST00000698863.1:c.1680C>A	ENSP00000513991.1:p.Gly560=
ENST00000698864.1:n.2241C>A
ENST00000698865.1:c.1701C>A	ENSP00000513992.1:p.Gly567=
ENST00000698866.1:c.*1468C>A	ENSP00000513993.1:n.*1468C>A
ENST00000698867.1:n.5655C>A
ENST00000698868.1:c.1545C>A	ENSP00000513994.1:p.Gly515=
ENST00000698869.1:c.1446C>A	ENSP00000513995.1:p.Gly482=
ENST00000698870.1:c.1680C>A	ENSP00000513996.1:p.Gly560=
ENST00000698871.1:n.2203C>A
ENST00000698872.1:c.*469C>A	ENSP00000513997.1:n.*469C>A
ENST00000698873.1:c.*875C>A	ENSP00000513998.1:n.*875C>A
ENST00000698874.1:c.1140C>A	ENSP00000513999.1:p.Gly380=
ENST00000698875.1:n.1540C>A
ENST00000698876.1:n.1728C>A
ENST00000698877.1:n.1248C>A
ENST00000698878.1:c.1674C>A	ENSP00000514000.1:p.Gly558=
ENST00000698880.1:c.1548C>A
ENST00000345728.10:c.1680C>A MANE Select	ENSP00000339950.5:p.Gly560=
ENST00000279227.9:c.1692C>A	ENSP00000279227.5:p.Gly564=
ENST00000345728.9:c.1680C>A	ENSP00000339950.5:p.Gly560=
ENST00000540554.1:n.316C>A
ENST00000545896.1:c.243C>A	ENSP00000440209.1:p.Gly81=
NM_031471.5:c.1680C>A	NP_113659.3:p.Gly560=
NM_178443.2:c.1692C>A , LRG_180t1:c.1692C>A	NP_848537.1:p.Gly564=
XM_011545294.1:c.1692C>A	XP_011543596.1:p.Gly564=
XM_011545295.1:c.1152C>A	XP_011543597.1:p.Gly384=
XM_011545296.1:c.1152C>A	XP_011543598.1:p.Gly384=
XM_011545294.3:c.1692C>A	XP_011543596.1:p.Gly564=
XM_011545295.2:c.1152C>A	XP_011543597.1:p.Gly384=
XM_017018398.2:c.1680C>A	XP_016873887.1:p.Gly560=
XM_017018399.1:c.1140C>A	XP_016873888.1:p.Gly380=
NM_031471.6:c.1680C>A MANE Select	NP_113659.3:p.Gly560=
NM_001382361.1:c.1680C>A	NP_001369290.1:p.Gly560=
NM_001382362.1:c.1692C>A	NP_001369291.1:p.Gly564=
NM_001382363.1:c.1140C>A	NP_001369292.1:p.Gly380=
NM_001382364.1:c.1152C>A	NP_001369293.1:p.Gly384=
NM_001382448.1:c.1680C>A	NP_001369377.1:p.Gly560=
NM_178443.3:c.1692C>A	NP_848537.1:p.Gly564=