Canonical Allele Identifier: CA381089474

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990535G>T (hg19) ; chr11:g.64223063G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223063G>T , CM000673.2:g.64223063G>T	GRCh38
NC_000011.9:g.63990535G>T , CM000673.1:g.63990535G>T	GRCh37
NC_000011.8:g.63747111G>T	NCBI36
NG_016360.1:g.21384G>T , LRG_180:g.21384G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1698G>T	ENSP00000279227.5:p.Arg566Ser
ENST00000540554.2:n.3210G>T
ENST00000541252.2:c.1146G>T	ENSP00000438885.2:p.Arg382Ser
ENST00000544997.6:c.1686G>T	ENSP00000445778.2:p.Arg562Ser
ENST00000545896.2:c.250G>T	ENSP00000440209.2:p.Glu84Ter
ENST00000546255.2:n.1990G>T
ENST00000698845.1:c.*881G>T	ENSP00000513981.1:n.*881G>T
ENST00000698846.1:n.1932G>T
ENST00000698847.1:c.*1091G>T	ENSP00000513982.1:n.*1091G>T
ENST00000698850.1:n.3707G>T
ENST00000698852.1:c.1686G>T	ENSP00000513984.1:p.Arg562Ser
ENST00000698853.1:c.*915G>T	ENSP00000513985.1:n.*915G>T
ENST00000698854.1:c.*1016G>T	ENSP00000513986.1:n.*1016G>T
ENST00000698855.1:n.3338G>T
ENST00000698856.1:n.3032G>T
ENST00000698859.1:n.2196G>T
ENST00000698860.1:c.1698G>T	ENSP00000513988.1:p.Arg566Ser
ENST00000698861.1:c.1686G>T	ENSP00000513989.1:p.Arg562Ser
ENST00000698862.1:c.*982G>T	ENSP00000513990.1:n.*982G>T
ENST00000698863.1:c.1686G>T	ENSP00000513991.1:p.Arg562Ser
ENST00000698864.1:n.2247G>T
ENST00000698865.1:c.1707G>T	ENSP00000513992.1:p.Arg569Ser
ENST00000698866.1:c.*1474G>T	ENSP00000513993.1:n.*1474G>T
ENST00000698867.1:n.5661G>T
ENST00000698868.1:c.1551G>T	ENSP00000513994.1:p.Arg517Ser
ENST00000698869.1:c.1452G>T	ENSP00000513995.1:p.Arg484Ser
ENST00000698870.1:c.1686G>T	ENSP00000513996.1:p.Arg562Ser
ENST00000698871.1:n.2209G>T
ENST00000698872.1:c.*475G>T	ENSP00000513997.1:n.*475G>T
ENST00000698873.1:c.*881G>T	ENSP00000513998.1:n.*881G>T
ENST00000698874.1:c.1146G>T	ENSP00000513999.1:p.Arg382Ser
ENST00000698875.1:n.1546G>T
ENST00000698876.1:n.1734G>T
ENST00000698877.1:n.1254G>T
ENST00000698878.1:c.1680G>T	ENSP00000514000.1:p.Arg560Ser
ENST00000698880.1:c.1554G>T
ENST00000345728.10:c.1686G>T MANE Select	ENSP00000339950.5:p.Arg562Ser
ENST00000279227.9:c.1698G>T	ENSP00000279227.5:p.Arg566Ser
ENST00000345728.9:c.1686G>T	ENSP00000339950.5:p.Arg562Ser
ENST00000540554.1:n.322G>T
ENST00000545896.1:c.249G>T	ENSP00000440209.1:p.Arg83Ser
NM_031471.5:c.1686G>T	NP_113659.3:p.Arg562Ser
NM_178443.2:c.1698G>T , LRG_180t1:c.1698G>T	NP_848537.1:p.Arg566Ser
XM_011545294.1:c.1698G>T	XP_011543596.1:p.Arg566Ser
XM_011545295.1:c.1158G>T	XP_011543597.1:p.Arg386Ser
XM_011545296.1:c.1158G>T	XP_011543598.1:p.Arg386Ser
XM_011545294.3:c.1698G>T	XP_011543596.1:p.Arg566Ser
XM_011545295.2:c.1158G>T	XP_011543597.1:p.Arg386Ser
XM_017018398.2:c.1686G>T	XP_016873887.1:p.Arg562Ser
XM_017018399.1:c.1146G>T	XP_016873888.1:p.Arg382Ser
NM_031471.6:c.1686G>T MANE Select	NP_113659.3:p.Arg562Ser
NM_001382361.1:c.1686G>T	NP_001369290.1:p.Arg562Ser
NM_001382362.1:c.1698G>T	NP_001369291.1:p.Arg566Ser
NM_001382363.1:c.1146G>T	NP_001369292.1:p.Arg382Ser
NM_001382364.1:c.1158G>T	NP_001369293.1:p.Arg386Ser
NM_001382448.1:c.1686G>T	NP_001369377.1:p.Arg562Ser
NM_178443.3:c.1698G>T	NP_848537.1:p.Arg566Ser