Canonical Allele Identifier: CA381089449

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990530A>T (hg19) ; chr11:g.64223058A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223058A>T , CM000673.2:g.64223058A>T	GRCh38
NC_000011.9:g.63990530A>T , CM000673.1:g.63990530A>T	GRCh37
NC_000011.8:g.63747106A>T	NCBI36
NG_016360.1:g.21379A>T , LRG_180:g.21379A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1693A>T	ENSP00000279227.5:p.Ser565Cys
ENST00000540554.2:n.3205A>T
ENST00000541252.2:c.1141A>T	ENSP00000438885.2:p.Ser381Cys
ENST00000544997.6:c.1681A>T	ENSP00000445778.2:p.Ser561Cys
ENST00000545896.2:c.245A>T	ENSP00000440209.2:p.Gln82Leu
ENST00000546255.2:n.1985A>T
ENST00000698845.1:c.*876A>T	ENSP00000513981.1:n.*876A>T
ENST00000698846.1:n.1927A>T
ENST00000698847.1:c.*1086A>T	ENSP00000513982.1:n.*1086A>T
ENST00000698850.1:n.3702A>T
ENST00000698852.1:c.1681A>T	ENSP00000513984.1:p.Ser561Cys
ENST00000698853.1:c.*910A>T	ENSP00000513985.1:n.*910A>T
ENST00000698854.1:c.*1011A>T	ENSP00000513986.1:n.*1011A>T
ENST00000698855.1:n.3333A>T
ENST00000698856.1:n.3027A>T
ENST00000698859.1:n.2191A>T
ENST00000698860.1:c.1693A>T	ENSP00000513988.1:p.Ser565Cys
ENST00000698861.1:c.1681A>T	ENSP00000513989.1:p.Ser561Cys
ENST00000698862.1:c.*977A>T	ENSP00000513990.1:n.*977A>T
ENST00000698863.1:c.1681A>T	ENSP00000513991.1:p.Ser561Cys
ENST00000698864.1:n.2242A>T
ENST00000698865.1:c.1702A>T	ENSP00000513992.1:p.Ser568Cys
ENST00000698866.1:c.*1469A>T	ENSP00000513993.1:n.*1469A>T
ENST00000698867.1:n.5656A>T
ENST00000698868.1:c.1546A>T	ENSP00000513994.1:p.Ser516Cys
ENST00000698869.1:c.1447A>T	ENSP00000513995.1:p.Ser483Cys
ENST00000698870.1:c.1681A>T	ENSP00000513996.1:p.Ser561Cys
ENST00000698871.1:n.2204A>T
ENST00000698872.1:c.*470A>T	ENSP00000513997.1:n.*470A>T
ENST00000698873.1:c.*876A>T	ENSP00000513998.1:n.*876A>T
ENST00000698874.1:c.1141A>T	ENSP00000513999.1:p.Ser381Cys
ENST00000698875.1:n.1541A>T
ENST00000698876.1:n.1729A>T
ENST00000698877.1:n.1249A>T
ENST00000698878.1:c.1675A>T	ENSP00000514000.1:p.Ser559Cys
ENST00000698880.1:c.1549A>T
ENST00000345728.10:c.1681A>T MANE Select	ENSP00000339950.5:p.Ser561Cys
ENST00000279227.9:c.1693A>T	ENSP00000279227.5:p.Ser565Cys
ENST00000345728.9:c.1681A>T	ENSP00000339950.5:p.Ser561Cys
ENST00000540554.1:n.317A>T
ENST00000545896.1:c.244A>T	ENSP00000440209.1:p.Ser82Cys
NM_031471.5:c.1681A>T	NP_113659.3:p.Ser561Cys
NM_178443.2:c.1693A>T , LRG_180t1:c.1693A>T	NP_848537.1:p.Ser565Cys
XM_011545294.1:c.1693A>T	XP_011543596.1:p.Ser565Cys
XM_011545295.1:c.1153A>T	XP_011543597.1:p.Ser385Cys
XM_011545296.1:c.1153A>T	XP_011543598.1:p.Ser385Cys
XM_011545294.3:c.1693A>T	XP_011543596.1:p.Ser565Cys
XM_011545295.2:c.1153A>T	XP_011543597.1:p.Ser385Cys
XM_017018398.2:c.1681A>T	XP_016873887.1:p.Ser561Cys
XM_017018399.1:c.1141A>T	XP_016873888.1:p.Ser381Cys
NM_031471.6:c.1681A>T MANE Select	NP_113659.3:p.Ser561Cys
NM_001382361.1:c.1681A>T	NP_001369290.1:p.Ser561Cys
NM_001382362.1:c.1693A>T	NP_001369291.1:p.Ser565Cys
NM_001382363.1:c.1141A>T	NP_001369292.1:p.Ser381Cys
NM_001382364.1:c.1153A>T	NP_001369293.1:p.Ser385Cys
NM_001382448.1:c.1681A>T	NP_001369377.1:p.Ser561Cys
NM_178443.3:c.1693A>T	NP_848537.1:p.Ser565Cys