Canonical Allele Identifier: CA381086938

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987695G>C (hg19) ; chr11:g.64220223G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220223G>C , CM000673.2:g.64220223G>C	GRCh38
NC_000011.9:g.63987695G>C , CM000673.1:g.63987695G>C	GRCh37
NC_000011.8:g.63744271G>C	NCBI36
NG_016360.1:g.18544G>C , LRG_180:g.18544G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1220G>C	ENSP00000279227.5:p.Cys407Ser
ENST00000540554.2:n.2277G>C
ENST00000541252.2:c.668G>C	ENSP00000438885.2:p.Cys223Ser
ENST00000541326.6:n.520G>C
ENST00000544997.6:c.1208G>C	ENSP00000445778.2:p.Cys403Ser
ENST00000546255.2:n.1403G>C
ENST00000698845.1:c.*403G>C	ENSP00000513981.1:n.*403G>C
ENST00000698846.1:n.1345G>C
ENST00000698847.1:c.*613G>C	ENSP00000513982.1:n.*613G>C
ENST00000698848.1:n.397G>C
ENST00000698849.1:n.328G>C
ENST00000698850.1:n.867G>C
ENST00000698852.1:c.1208G>C	ENSP00000513984.1:p.Cys403Ser
ENST00000698853.1:c.*437G>C	ENSP00000513985.1:n.*437G>C
ENST00000698854.1:c.*538G>C	ENSP00000513986.1:n.*538G>C
ENST00000698855.1:n.2860G>C
ENST00000698856.1:n.2445G>C
ENST00000698859.1:n.1372G>C
ENST00000698860.1:c.1220G>C	ENSP00000513988.1:p.Cys407Ser
ENST00000698861.1:c.1208G>C	ENSP00000513989.1:p.Cys403Ser
ENST00000698862.1:c.*504G>C	ENSP00000513990.1:n.*504G>C
ENST00000698863.1:c.1208G>C	ENSP00000513991.1:p.Cys403Ser
ENST00000698864.1:n.1314G>C
ENST00000698865.1:c.1229G>C	ENSP00000513992.1:p.Cys410Ser
ENST00000698866.1:c.*613G>C	ENSP00000513993.1:n.*613G>C
ENST00000698867.1:n.5183G>C
ENST00000698868.1:c.1073G>C	ENSP00000513994.1:p.Cys358Ser
ENST00000698869.1:c.1208G>C	ENSP00000513995.1:p.Cys403Ser
ENST00000698870.1:c.1208G>C	ENSP00000513996.1:p.Cys403Ser
ENST00000698871.1:n.1731G>C
ENST00000698872.1:c.663G>C	ENSP00000513997.1:p.Leu221=
ENST00000698873.1:c.*403G>C	ENSP00000513998.1:n.*403G>C
ENST00000698874.1:c.668G>C	ENSP00000513999.1:p.Cys223Ser
ENST00000698875.1:n.1068G>C
ENST00000698876.1:n.1147G>C
ENST00000698877.1:n.776G>C
ENST00000698878.1:c.1208G>C	ENSP00000514000.1:p.Cys403Ser
ENST00000698880.1:c.1048G>C
ENST00000345728.10:c.1208G>C MANE Select	ENSP00000339950.5:p.Cys403Ser
ENST00000279227.9:c.1220G>C	ENSP00000279227.5:p.Cys407Ser
ENST00000345728.9:c.1208G>C	ENSP00000339950.5:p.Cys403Ser
ENST00000540957.1:n.361G>C
ENST00000541326.5:n.515G>C
NM_031471.5:c.1208G>C	NP_113659.3:p.Cys403Ser
NM_178443.2:c.1220G>C , LRG_180t1:c.1220G>C	NP_848537.1:p.Cys407Ser
XM_011545294.1:c.1220G>C	XP_011543596.1:p.Cys407Ser
XM_011545295.1:c.680G>C	XP_011543597.1:p.Cys227Ser
XM_011545296.1:c.680G>C	XP_011543598.1:p.Cys227Ser
XM_011545294.3:c.1220G>C	XP_011543596.1:p.Cys407Ser
XM_011545295.2:c.680G>C	XP_011543597.1:p.Cys227Ser
XM_017018398.2:c.1208G>C	XP_016873887.1:p.Cys403Ser
XM_017018399.1:c.668G>C	XP_016873888.1:p.Cys223Ser
NM_031471.6:c.1208G>C MANE Select	NP_113659.3:p.Cys403Ser
NM_001382361.1:c.1208G>C	NP_001369290.1:p.Cys403Ser
NM_001382362.1:c.1220G>C	NP_001369291.1:p.Cys407Ser
NM_001382363.1:c.668G>C	NP_001369292.1:p.Cys223Ser
NM_001382364.1:c.680G>C	NP_001369293.1:p.Cys227Ser
NM_001382448.1:c.1208G>C	NP_001369377.1:p.Cys403Ser
NM_178443.3:c.1220G>C	NP_848537.1:p.Cys407Ser