Canonical Allele Identifier: CA381087589

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987976C>G (hg19) ; chr11:g.64220504C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220504C>G , CM000673.2:g.64220504C>G	GRCh38
NC_000011.9:g.63987976C>G , CM000673.1:g.63987976C>G	GRCh37
NC_000011.8:g.63744552C>G	NCBI36
NG_016360.1:g.18825C>G , LRG_180:g.18825C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1392C>G	ENSP00000279227.5:p.Ser464Arg
ENST00000540554.2:n.2558C>G
ENST00000541252.2:c.840C>G	ENSP00000438885.2:p.Ser280Arg
ENST00000541326.6:n.801C>G
ENST00000544997.6:c.1380C>G	ENSP00000445778.2:p.Ser460Arg
ENST00000545896.2:c.69C>G	ENSP00000440209.2:p.Ser23Arg
ENST00000546255.2:n.1684C>G
ENST00000698845.1:c.*575C>G	ENSP00000513981.1:n.*575C>G
ENST00000698846.1:n.1626C>G
ENST00000698847.1:c.*785C>G	ENSP00000513982.1:n.*785C>G
ENST00000698849.1:n.500C>G
ENST00000698850.1:n.1148C>G
ENST00000698852.1:c.1380C>G	ENSP00000513984.1:p.Ser460Arg
ENST00000698853.1:c.*609C>G	ENSP00000513985.1:n.*609C>G
ENST00000698854.1:c.*710C>G	ENSP00000513986.1:n.*710C>G
ENST00000698855.1:n.3032C>G
ENST00000698856.1:n.2726C>G
ENST00000698859.1:n.1544C>G
ENST00000698860.1:c.1392C>G	ENSP00000513988.1:p.Ser464Arg
ENST00000698861.1:c.1380C>G	ENSP00000513989.1:p.Ser460Arg
ENST00000698862.1:c.*676C>G	ENSP00000513990.1:n.*676C>G
ENST00000698863.1:c.1380C>G	ENSP00000513991.1:p.Ser460Arg
ENST00000698864.1:n.1595C>G
ENST00000698865.1:c.1401C>G	ENSP00000513992.1:p.Ser467Arg
ENST00000698866.1:c.*894C>G	ENSP00000513993.1:n.*894C>G
ENST00000698867.1:n.5355C>G
ENST00000698868.1:c.1245C>G	ENSP00000513994.1:p.Ser415Arg
ENST00000698869.1:c.1311+178C>G	ENSP00000513995.1:n.1311+178C>G
ENST00000698870.1:c.1380C>G	ENSP00000513996.1:p.Ser460Arg
ENST00000698871.1:n.1903C>G
ENST00000698872.1:c.*169C>G	ENSP00000513997.1:n.*169C>G
ENST00000698873.1:c.*575C>G	ENSP00000513998.1:n.*575C>G
ENST00000698874.1:c.840C>G	ENSP00000513999.1:p.Ser280Arg
ENST00000698875.1:n.1240C>G
ENST00000698876.1:n.1428C>G
ENST00000698877.1:n.948C>G
ENST00000698878.1:c.1374C>G	ENSP00000514000.1:p.Ser458Arg
ENST00000698880.1:c.1248C>G
ENST00000345728.10:c.1380C>G MANE Select	ENSP00000339950.5:p.Ser460Arg
ENST00000279227.9:c.1392C>G	ENSP00000279227.5:p.Ser464Arg
ENST00000345728.9:c.1380C>G	ENSP00000339950.5:p.Ser460Arg
ENST00000541326.5:n.796C>G
ENST00000545896.1:c.68C>G	ENSP00000440209.1:p.Ala23Gly
NM_031471.5:c.1380C>G	NP_113659.3:p.Ser460Arg
NM_178443.2:c.1392C>G , LRG_180t1:c.1392C>G	NP_848537.1:p.Ser464Arg
XM_011545294.1:c.1392C>G	XP_011543596.1:p.Ser464Arg
XM_011545295.1:c.852C>G	XP_011543597.1:p.Ser284Arg
XM_011545296.1:c.852C>G	XP_011543598.1:p.Ser284Arg
XM_011545294.3:c.1392C>G	XP_011543596.1:p.Ser464Arg
XM_011545295.2:c.852C>G	XP_011543597.1:p.Ser284Arg
XM_017018398.2:c.1380C>G	XP_016873887.1:p.Ser460Arg
XM_017018399.1:c.840C>G	XP_016873888.1:p.Ser280Arg
NM_031471.6:c.1380C>G MANE Select	NP_113659.3:p.Ser460Arg
NM_001382361.1:c.1380C>G	NP_001369290.1:p.Ser460Arg
NM_001382362.1:c.1392C>G	NP_001369291.1:p.Ser464Arg
NM_001382363.1:c.840C>G	NP_001369292.1:p.Ser280Arg
NM_001382364.1:c.852C>G	NP_001369293.1:p.Ser284Arg
NM_001382448.1:c.1380C>G	NP_001369377.1:p.Ser460Arg
NM_178443.3:c.1392C>G	NP_848537.1:p.Ser464Arg