Canonical Allele Identifier: CA381087549

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987961C>G (hg19) ; chr11:g.64220489C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220489C>G , CM000673.2:g.64220489C>G	GRCh38
NC_000011.9:g.63987961C>G , CM000673.1:g.63987961C>G	GRCh37
NC_000011.8:g.63744537C>G	NCBI36
NG_016360.1:g.18810C>G , LRG_180:g.18810C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1377C>G	ENSP00000279227.5:p.Arg459=
ENST00000540554.2:n.2543C>G
ENST00000541252.2:c.825C>G	ENSP00000438885.2:p.Arg275=
ENST00000541326.6:n.786C>G
ENST00000544997.6:c.1365C>G	ENSP00000445778.2:p.Arg455=
ENST00000545896.2:c.54C>G	ENSP00000440209.2:p.Arg18=
ENST00000546255.2:n.1669C>G
ENST00000698845.1:c.*560C>G	ENSP00000513981.1:n.*560C>G
ENST00000698846.1:n.1611C>G
ENST00000698847.1:c.*770C>G	ENSP00000513982.1:n.*770C>G
ENST00000698849.1:n.485C>G
ENST00000698850.1:n.1133C>G
ENST00000698852.1:c.1365C>G	ENSP00000513984.1:p.Arg455=
ENST00000698853.1:c.*594C>G	ENSP00000513985.1:n.*594C>G
ENST00000698854.1:c.*695C>G	ENSP00000513986.1:n.*695C>G
ENST00000698855.1:n.3017C>G
ENST00000698856.1:n.2711C>G
ENST00000698859.1:n.1529C>G
ENST00000698860.1:c.1377C>G	ENSP00000513988.1:p.Arg459=
ENST00000698861.1:c.1365C>G	ENSP00000513989.1:p.Arg455=
ENST00000698862.1:c.*661C>G	ENSP00000513990.1:n.*661C>G
ENST00000698863.1:c.1365C>G	ENSP00000513991.1:p.Arg455=
ENST00000698864.1:n.1580C>G
ENST00000698865.1:c.1386C>G	ENSP00000513992.1:p.Arg462=
ENST00000698866.1:c.*879C>G	ENSP00000513993.1:n.*879C>G
ENST00000698867.1:n.5340C>G
ENST00000698868.1:c.1230C>G	ENSP00000513994.1:p.Arg410=
ENST00000698869.1:c.1311+163C>G	ENSP00000513995.1:n.1311+163C>G
ENST00000698870.1:c.1365C>G	ENSP00000513996.1:p.Arg455=
ENST00000698871.1:n.1888C>G
ENST00000698872.1:c.*154C>G	ENSP00000513997.1:n.*154C>G
ENST00000698873.1:c.*560C>G	ENSP00000513998.1:n.*560C>G
ENST00000698874.1:c.825C>G	ENSP00000513999.1:p.Arg275=
ENST00000698875.1:n.1225C>G
ENST00000698876.1:n.1413C>G
ENST00000698877.1:n.933C>G
ENST00000698878.1:c.1359C>G	ENSP00000514000.1:p.Arg453=
ENST00000698880.1:c.1233C>G
ENST00000345728.10:c.1365C>G MANE Select	ENSP00000339950.5:p.Arg455=
ENST00000279227.9:c.1377C>G	ENSP00000279227.5:p.Arg459=
ENST00000345728.9:c.1365C>G	ENSP00000339950.5:p.Arg455=
ENST00000541326.5:n.781C>G
ENST00000545896.1:c.53C>G	ENSP00000440209.1:p.Ala18Gly
NM_031471.5:c.1365C>G	NP_113659.3:p.Arg455=
NM_178443.2:c.1377C>G , LRG_180t1:c.1377C>G	NP_848537.1:p.Arg459=
XM_011545294.1:c.1377C>G	XP_011543596.1:p.Arg459=
XM_011545295.1:c.837C>G	XP_011543597.1:p.Arg279=
XM_011545296.1:c.837C>G	XP_011543598.1:p.Arg279=
XM_011545294.3:c.1377C>G	XP_011543596.1:p.Arg459=
XM_011545295.2:c.837C>G	XP_011543597.1:p.Arg279=
XM_017018398.2:c.1365C>G	XP_016873887.1:p.Arg455=
XM_017018399.1:c.825C>G	XP_016873888.1:p.Arg275=
NM_031471.6:c.1365C>G MANE Select	NP_113659.3:p.Arg455=
NM_001382361.1:c.1365C>G	NP_001369290.1:p.Arg455=
NM_001382362.1:c.1377C>G	NP_001369291.1:p.Arg459=
NM_001382363.1:c.825C>G	NP_001369292.1:p.Arg275=
NM_001382364.1:c.837C>G	NP_001369293.1:p.Arg279=
NM_001382448.1:c.1365C>G	NP_001369377.1:p.Arg455=
NM_178443.3:c.1377C>G	NP_848537.1:p.Arg459=