Canonical Allele Identifier: CA381087850

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63988031G>C (hg19) ; chr11:g.64220559G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220559G>C , CM000673.2:g.64220559G>C	GRCh38
NC_000011.9:g.63988031G>C , CM000673.1:g.63988031G>C	GRCh37
NC_000011.8:g.63744607G>C	NCBI36
NG_016360.1:g.18880G>C , LRG_180:g.18880G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000279227.10:c.1447G>C	ENSP00000279227.5:p.Gly483Arg
ENST00000540554.2:n.2613G>C
ENST00000541252.2:c.895G>C	ENSP00000438885.2:p.Gly299Arg
ENST00000541326.6:n.856G>C
ENST00000544997.6:c.1435G>C	ENSP00000445778.2:p.Gly479Arg
ENST00000545896.2:c.124G>C	ENSP00000440209.2:p.Gly42Arg
ENST00000546255.2:n.1739G>C
ENST00000698845.1:c.*630G>C	ENSP00000513981.1:n.*630G>C
ENST00000698846.1:n.1681G>C
ENST00000698847.1:c.*840G>C	ENSP00000513982.1:n.*840G>C
ENST00000698849.1:n.555G>C
ENST00000698850.1:n.1203G>C
ENST00000698852.1:c.1435G>C	ENSP00000513984.1:p.Gly479Arg
ENST00000698853.1:c.*664G>C	ENSP00000513985.1:n.*664G>C
ENST00000698854.1:c.*765G>C	ENSP00000513986.1:n.*765G>C
ENST00000698855.1:n.3087G>C
ENST00000698856.1:n.2781G>C
ENST00000698859.1:n.1599G>C
ENST00000698860.1:c.1447G>C	ENSP00000513988.1:p.Gly483Arg
ENST00000698861.1:c.1435G>C	ENSP00000513989.1:p.Gly479Arg
ENST00000698862.1:c.*731G>C	ENSP00000513990.1:n.*731G>C
ENST00000698863.1:c.1435G>C	ENSP00000513991.1:p.Gly479Arg
ENST00000698864.1:n.1650G>C
ENST00000698865.1:c.1456G>C	ENSP00000513992.1:p.Gly486Arg
ENST00000698866.1:c.*949G>C	ENSP00000513993.1:n.*949G>C
ENST00000698867.1:n.5410G>C
ENST00000698868.1:c.1300G>C	ENSP00000513994.1:p.Gly434Arg
ENST00000698869.1:c.1311+233G>C	ENSP00000513995.1:n.1311+233G>C
ENST00000698870.1:c.1435G>C	ENSP00000513996.1:p.Gly479Arg
ENST00000698871.1:n.1958G>C
ENST00000698872.1:c.*224G>C	ENSP00000513997.1:n.*224G>C
ENST00000698873.1:c.*630G>C	ENSP00000513998.1:n.*630G>C
ENST00000698874.1:c.895G>C	ENSP00000513999.1:p.Gly299Arg
ENST00000698875.1:n.1295G>C
ENST00000698876.1:n.1483G>C
ENST00000698877.1:n.1003G>C
ENST00000698878.1:c.1429G>C	ENSP00000514000.1:p.Gly477Arg
ENST00000698880.1:c.1303G>C
ENST00000345728.10:c.1435G>C MANE Select	ENSP00000339950.5:p.Gly479Arg
ENST00000279227.9:c.1447G>C	ENSP00000279227.5:p.Gly483Arg
ENST00000345728.9:c.1435G>C	ENSP00000339950.5:p.Gly479Arg
ENST00000541326.5:n.851G>C
ENST00000545896.1:c.123G>C	ENSP00000440209.1:p.Arg41=
NM_031471.5:c.1435G>C	NP_113659.3:p.Gly479Arg
NM_178443.2:c.1447G>C , LRG_180t1:c.1447G>C	NP_848537.1:p.Gly483Arg
XM_011545294.1:c.1447G>C	XP_011543596.1:p.Gly483Arg
XM_011545295.1:c.907G>C	XP_011543597.1:p.Gly303Arg
XM_011545296.1:c.907G>C	XP_011543598.1:p.Gly303Arg
XM_011545294.3:c.1447G>C	XP_011543596.1:p.Gly483Arg
XM_011545295.2:c.907G>C	XP_011543597.1:p.Gly303Arg
XM_017018398.2:c.1435G>C	XP_016873887.1:p.Gly479Arg
XM_017018399.1:c.895G>C	XP_016873888.1:p.Gly299Arg
NM_031471.6:c.1435G>C MANE Select	NP_113659.3:p.Gly479Arg
NM_001382361.1:c.1435G>C	NP_001369290.1:p.Gly479Arg
NM_001382362.1:c.1447G>C	NP_001369291.1:p.Gly483Arg
NM_001382363.1:c.895G>C	NP_001369292.1:p.Gly299Arg
NM_001382364.1:c.907G>C	NP_001369293.1:p.Gly303Arg
NM_001382448.1:c.1435G>C	NP_001369377.1:p.Gly479Arg
NM_178443.3:c.1447G>C	NP_848537.1:p.Gly483Arg