Canonical Allele Identifier: CA475151829

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990622C>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1785C>T	ENSP00000279227.5:p.Ser595=
ENST00000540554.2:n.3297C>T
ENST00000541252.2:c.1233C>T	ENSP00000438885.2:p.Ser411=
ENST00000544997.6:c.1773C>T	ENSP00000445778.2:p.Ser591=
ENST00000545896.2:c.337C>T	ENSP00000440209.2:p.Gln113Ter
ENST00000546255.2:n.2077C>T
ENST00000698845.1:c.*968C>T	ENSP00000513981.1:n.*968C>T
ENST00000698846.1:n.2019C>T
ENST00000698847.1:c.*1178C>T	ENSP00000513982.1:n.*1178C>T
ENST00000698850.1:n.3794C>T
ENST00000698852.1:c.1773C>T	ENSP00000513984.1:p.Ser591=
ENST00000698853.1:c.*1002C>T	ENSP00000513985.1:n.*1002C>T
ENST00000698854.1:c.*1103C>T	ENSP00000513986.1:n.*1103C>T
ENST00000698855.1:n.3425C>T
ENST00000698856.1:n.3119C>T
ENST00000698859.1:n.2283C>T
ENST00000698860.1:c.1785C>T	ENSP00000513988.1:p.Ser595=
ENST00000698861.1:c.1773C>T	ENSP00000513989.1:p.Ser591=
ENST00000698862.1:c.*1069C>T	ENSP00000513990.1:n.*1069C>T
ENST00000698863.1:c.1773C>T	ENSP00000513991.1:p.Ser591=
ENST00000698864.1:n.2334C>T
ENST00000698865.1:c.1794C>T	ENSP00000513992.1:p.Ser598=
ENST00000698866.1:c.*1561C>T	ENSP00000513993.1:n.*1561C>T
ENST00000698867.1:n.5748C>T
ENST00000698868.1:c.1638C>T	ENSP00000513994.1:p.Ser546=
ENST00000698869.1:c.1539C>T	ENSP00000513995.1:p.Ser513=
ENST00000698870.1:c.1773C>T	ENSP00000513996.1:p.Ser591=
ENST00000698871.1:n.2296C>T
ENST00000698872.1:c.*562C>T	ENSP00000513997.1:n.*562C>T
ENST00000698873.1:c.*968C>T	ENSP00000513998.1:n.*968C>T
ENST00000698874.1:c.1233C>T	ENSP00000513999.1:p.Ser411=
ENST00000698875.1:n.1633C>T
ENST00000698876.1:n.1821C>T
ENST00000698877.1:n.1341C>T
ENST00000698878.1:c.1767C>T	ENSP00000514000.1:p.Ser589=
ENST00000698880.1:c.1641C>T
ENST00000345728.10:c.1773C>T MANE Select	ENSP00000339950.5:p.Ser591=
ENST00000279227.9:c.1785C>T	ENSP00000279227.5:p.Ser595=
ENST00000345728.9:c.1773C>T	ENSP00000339950.5:p.Ser591=
ENST00000545896.1:c.336C>T	ENSP00000440209.1:p.Ser112=
NM_031471.5:c.1773C>T	NP_113659.3:p.Ser591=
NM_178443.2:c.1785C>T , LRG_180t1:c.1785C>T	NP_848537.1:p.Ser595=
XM_011545294.1:c.1785C>T	XP_011543596.1:p.Ser595=
XM_011545295.1:c.1245C>T	XP_011543597.1:p.Ser415=
XM_011545296.1:c.1245C>T	XP_011543598.1:p.Ser415=
XM_011545294.3:c.1785C>T	XP_011543596.1:p.Ser595=
XM_011545295.2:c.1245C>T	XP_011543597.1:p.Ser415=
XM_017018398.2:c.1773C>T	XP_016873887.1:p.Ser591=
XM_017018399.1:c.1233C>T	XP_016873888.1:p.Ser411=
NM_031471.6:c.1773C>T MANE Select	NP_113659.3:p.Ser591=
NM_001382361.1:c.1773C>T	NP_001369290.1:p.Ser591=
NM_001382362.1:c.1785C>T	NP_001369291.1:p.Ser595=
NM_001382363.1:c.1233C>T	NP_001369292.1:p.Ser411=
NM_001382364.1:c.1245C>T	NP_001369293.1:p.Ser415=
NM_001382448.1:c.1773C>T	NP_001369377.1:p.Ser591=
NM_178443.3:c.1785C>T	NP_848537.1:p.Ser595=