Canonical Allele Identifier: CA475151706

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987696T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220224T>C , CM000673.2:g.64220224T>C	GRCh38
NC_000011.9:g.63987696T>C , CM000673.1:g.63987696T>C	GRCh37
NC_000011.8:g.63744272T>C	NCBI36
NG_016360.1:g.18545T>C , LRG_180:g.18545T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1221T>C	ENSP00000279227.5:p.Cys407=
ENST00000540554.2:n.2278T>C
ENST00000541252.2:c.669T>C	ENSP00000438885.2:p.Cys223=
ENST00000541326.6:n.521T>C
ENST00000544997.6:c.1209T>C	ENSP00000445778.2:p.Cys403=
ENST00000546255.2:n.1404T>C
ENST00000698845.1:c.*404T>C	ENSP00000513981.1:n.*404T>C
ENST00000698846.1:n.1346T>C
ENST00000698847.1:c.*614T>C	ENSP00000513982.1:n.*614T>C
ENST00000698848.1:n.398T>C
ENST00000698849.1:n.329T>C
ENST00000698850.1:n.868T>C
ENST00000698852.1:c.1209T>C	ENSP00000513984.1:p.Cys403=
ENST00000698853.1:c.*438T>C	ENSP00000513985.1:n.*438T>C
ENST00000698854.1:c.*539T>C	ENSP00000513986.1:n.*539T>C
ENST00000698855.1:n.2861T>C
ENST00000698856.1:n.2446T>C
ENST00000698859.1:n.1373T>C
ENST00000698860.1:c.1221T>C	ENSP00000513988.1:p.Cys407=
ENST00000698861.1:c.1209T>C	ENSP00000513989.1:p.Cys403=
ENST00000698862.1:c.*505T>C	ENSP00000513990.1:n.*505T>C
ENST00000698863.1:c.1209T>C	ENSP00000513991.1:p.Cys403=
ENST00000698864.1:n.1315T>C
ENST00000698865.1:c.1230T>C	ENSP00000513992.1:p.Cys410=
ENST00000698866.1:c.*614T>C	ENSP00000513993.1:n.*614T>C
ENST00000698867.1:n.5184T>C
ENST00000698868.1:c.1074T>C	ENSP00000513994.1:p.Cys358=
ENST00000698869.1:c.1209T>C	ENSP00000513995.1:p.Cys403=
ENST00000698870.1:c.1209T>C	ENSP00000513996.1:p.Cys403=
ENST00000698871.1:n.1732T>C
ENST00000698872.1:c.664T>C	ENSP00000513997.1:p.Ter222Arg
ENST00000698873.1:c.*404T>C	ENSP00000513998.1:n.*404T>C
ENST00000698874.1:c.669T>C	ENSP00000513999.1:p.Cys223=
ENST00000698875.1:n.1069T>C
ENST00000698876.1:n.1148T>C
ENST00000698877.1:n.777T>C
ENST00000698878.1:c.1209T>C	ENSP00000514000.1:p.Cys403=
ENST00000698880.1:c.1049T>C
ENST00000345728.10:c.1209T>C MANE Select	ENSP00000339950.5:p.Cys403=
ENST00000279227.9:c.1221T>C	ENSP00000279227.5:p.Cys407=
ENST00000345728.9:c.1209T>C	ENSP00000339950.5:p.Cys403=
ENST00000540957.1:n.362T>C
ENST00000541326.5:n.516T>C
NM_031471.5:c.1209T>C	NP_113659.3:p.Cys403=
NM_178443.2:c.1221T>C , LRG_180t1:c.1221T>C	NP_848537.1:p.Cys407=
XM_011545294.1:c.1221T>C	XP_011543596.1:p.Cys407=
XM_011545295.1:c.681T>C	XP_011543597.1:p.Cys227=
XM_011545296.1:c.681T>C	XP_011543598.1:p.Cys227=
XM_011545294.3:c.1221T>C	XP_011543596.1:p.Cys407=
XM_011545295.2:c.681T>C	XP_011543597.1:p.Cys227=
XM_017018398.2:c.1209T>C	XP_016873887.1:p.Cys403=
XM_017018399.1:c.669T>C	XP_016873888.1:p.Cys223=
NM_031471.6:c.1209T>C MANE Select	NP_113659.3:p.Cys403=
NM_001382361.1:c.1209T>C	NP_001369290.1:p.Cys403=
NM_001382362.1:c.1221T>C	NP_001369291.1:p.Cys407=
NM_001382363.1:c.669T>C	NP_001369292.1:p.Cys223=
NM_001382364.1:c.681T>C	NP_001369293.1:p.Cys227=
NM_001382448.1:c.1209T>C	NP_001369377.1:p.Cys403=
NM_178443.3:c.1221T>C	NP_848537.1:p.Cys407=