Canonical Allele Identifier: CA381089959

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990622C>G (hg19) ; chr11:g.64223150C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223150C>G , CM000673.2:g.64223150C>G	GRCh38
NC_000011.9:g.63990622C>G , CM000673.1:g.63990622C>G	GRCh37
NC_000011.8:g.63747198C>G	NCBI36
NG_016360.1:g.21471C>G , LRG_180:g.21471C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1785C>G	ENSP00000279227.5:p.Ser595Arg
ENST00000540554.2:n.3297C>G
ENST00000541252.2:c.1233C>G	ENSP00000438885.2:p.Ser411Arg
ENST00000544997.6:c.1773C>G	ENSP00000445778.2:p.Ser591Arg
ENST00000545896.2:c.337C>G	ENSP00000440209.2:p.Gln113Glu
ENST00000546255.2:n.2077C>G
ENST00000698845.1:c.*968C>G	ENSP00000513981.1:n.*968C>G
ENST00000698846.1:n.2019C>G
ENST00000698847.1:c.*1178C>G	ENSP00000513982.1:n.*1178C>G
ENST00000698850.1:n.3794C>G
ENST00000698852.1:c.1773C>G	ENSP00000513984.1:p.Ser591Arg
ENST00000698853.1:c.*1002C>G	ENSP00000513985.1:n.*1002C>G
ENST00000698854.1:c.*1103C>G	ENSP00000513986.1:n.*1103C>G
ENST00000698855.1:n.3425C>G
ENST00000698856.1:n.3119C>G
ENST00000698859.1:n.2283C>G
ENST00000698860.1:c.1785C>G	ENSP00000513988.1:p.Ser595Arg
ENST00000698861.1:c.1773C>G	ENSP00000513989.1:p.Ser591Arg
ENST00000698862.1:c.*1069C>G	ENSP00000513990.1:n.*1069C>G
ENST00000698863.1:c.1773C>G	ENSP00000513991.1:p.Ser591Arg
ENST00000698864.1:n.2334C>G
ENST00000698865.1:c.1794C>G	ENSP00000513992.1:p.Ser598Arg
ENST00000698866.1:c.*1561C>G	ENSP00000513993.1:n.*1561C>G
ENST00000698867.1:n.5748C>G
ENST00000698868.1:c.1638C>G	ENSP00000513994.1:p.Ser546Arg
ENST00000698869.1:c.1539C>G	ENSP00000513995.1:p.Ser513Arg
ENST00000698870.1:c.1773C>G	ENSP00000513996.1:p.Ser591Arg
ENST00000698871.1:n.2296C>G
ENST00000698872.1:c.*562C>G	ENSP00000513997.1:n.*562C>G
ENST00000698873.1:c.*968C>G	ENSP00000513998.1:n.*968C>G
ENST00000698874.1:c.1233C>G	ENSP00000513999.1:p.Ser411Arg
ENST00000698875.1:n.1633C>G
ENST00000698876.1:n.1821C>G
ENST00000698877.1:n.1341C>G
ENST00000698878.1:c.1767C>G	ENSP00000514000.1:p.Ser589Arg
ENST00000698880.1:c.1641C>G
ENST00000345728.10:c.1773C>G MANE Select	ENSP00000339950.5:p.Ser591Arg
ENST00000279227.9:c.1785C>G	ENSP00000279227.5:p.Ser595Arg
ENST00000345728.9:c.1773C>G	ENSP00000339950.5:p.Ser591Arg
ENST00000545896.1:c.336C>G	ENSP00000440209.1:p.Ser112Arg
NM_031471.5:c.1773C>G	NP_113659.3:p.Ser591Arg
NM_178443.2:c.1785C>G , LRG_180t1:c.1785C>G	NP_848537.1:p.Ser595Arg
XM_011545294.1:c.1785C>G	XP_011543596.1:p.Ser595Arg
XM_011545295.1:c.1245C>G	XP_011543597.1:p.Ser415Arg
XM_011545296.1:c.1245C>G	XP_011543598.1:p.Ser415Arg
XM_011545294.3:c.1785C>G	XP_011543596.1:p.Ser595Arg
XM_011545295.2:c.1245C>G	XP_011543597.1:p.Ser415Arg
XM_017018398.2:c.1773C>G	XP_016873887.1:p.Ser591Arg
XM_017018399.1:c.1233C>G	XP_016873888.1:p.Ser411Arg
NM_031471.6:c.1773C>G MANE Select	NP_113659.3:p.Ser591Arg
NM_001382361.1:c.1773C>G	NP_001369290.1:p.Ser591Arg
NM_001382362.1:c.1785C>G	NP_001369291.1:p.Ser595Arg
NM_001382363.1:c.1233C>G	NP_001369292.1:p.Ser411Arg
NM_001382364.1:c.1245C>G	NP_001369293.1:p.Ser415Arg
NM_001382448.1:c.1773C>G	NP_001369377.1:p.Ser591Arg
NM_178443.3:c.1785C>G	NP_848537.1:p.Ser595Arg