Canonical Allele Identifier: CA1978639172
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220590G= , CM000673.2:g.64220590G= GRCh38
NC_000011.9:g.63988062G= , CM000673.1:g.63988062G= GRCh37
NC_000011.8:g.63744638G= NCBI36
NG_016360.1:g.18911G= , LRG_180:g.18911G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1478G= ENSP00000279227.5:p.Gly493=
ENST00000540554.2:n.2644G=
ENST00000541252.2:c.926G= ENSP00000438885.2:p.Gly309=
ENST00000541326.6:n.887G=
ENST00000544997.6:c.1466G= ENSP00000445778.2:p.Gly489=
ENST00000545896.2:c.155G= ENSP00000440209.2:p.Gly52=
ENST00000546255.2:n.1770G=
ENST00000698845.1:c.*661G= ENSP00000513981.1:n.*661G=
ENST00000698846.1:n.1712G=
ENST00000698847.1:c.*871G= ENSP00000513982.1:n.*871G=
ENST00000698849.1:n.586G=
ENST00000698850.1:n.1234G=
ENST00000698852.1:c.1466G= ENSP00000513984.1:p.Gly489=
ENST00000698853.1:c.*695G= ENSP00000513985.1:n.*695G=
ENST00000698854.1:c.*796G= ENSP00000513986.1:n.*796G=
ENST00000698855.1:n.3118G=
ENST00000698856.1:n.2812G=
ENST00000698859.1:n.1630G=
ENST00000698860.1:c.1478G= ENSP00000513988.1:p.Gly493=
ENST00000698861.1:c.1466G= ENSP00000513989.1:p.Gly489=
ENST00000698862.1:c.*762G= ENSP00000513990.1:n.*762G=
ENST00000698863.1:c.1466G= ENSP00000513991.1:p.Gly489=
ENST00000698864.1:n.1681G=
ENST00000698865.1:c.1487G= ENSP00000513992.1:p.Gly496=
ENST00000698866.1:c.*980G= ENSP00000513993.1:n.*980G=
ENST00000698867.1:n.5441G=
ENST00000698868.1:c.1331G= ENSP00000513994.1:p.Gly444=
ENST00000698869.1:c.1311+264G= ENSP00000513995.1:n.1311+264G=
ENST00000698870.1:c.1466G= ENSP00000513996.1:p.Gly489=
ENST00000698871.1:n.1989G=
ENST00000698872.1:c.*255G= ENSP00000513997.1:n.*255G=
ENST00000698873.1:c.*661G= ENSP00000513998.1:n.*661G=
ENST00000698874.1:c.926G= ENSP00000513999.1:p.Gly309=
ENST00000698875.1:n.1326G=
ENST00000698876.1:n.1514G=
ENST00000698877.1:n.1034G=
ENST00000698878.1:c.1460G= ENSP00000514000.1:p.Gly487=
ENST00000698880.1:c.1334G=
ENST00000345728.10:c.1466G= MANE Select ENSP00000339950.5:p.Gly489=
ENST00000279227.9:c.1478G= ENSP00000279227.5:p.Gly493=
ENST00000345728.9:c.1466G= ENSP00000339950.5:p.Gly489=
ENST00000541326.5:n.882G=
ENST00000545896.1:c.154G= ENSP00000440209.1:p.Ala52=
NM_031471.5:c.1466G= NP_113659.3:p.Gly489=
NM_178443.2:c.1478G= , LRG_180t1:c.1478G= NP_848537.1:p.Gly493=
XM_011545294.1:c.1478G= XP_011543596.1:p.Gly493=
XM_011545295.1:c.938G= XP_011543597.1:p.Gly313=
XM_011545296.1:c.938G= XP_011543598.1:p.Gly313=
XM_011545294.3:c.1478G= XP_011543596.1:p.Gly493=
XM_011545295.2:c.938G= XP_011543597.1:p.Gly313=
XM_017018398.2:c.1466G= XP_016873887.1:p.Gly489=
XM_017018399.1:c.926G= XP_016873888.1:p.Gly309=
NM_031471.6:c.1466G= MANE Select NP_113659.3:p.Gly489=
NM_001382361.1:c.1466G= NP_001369290.1:p.Gly489=
NM_001382362.1:c.1478G= NP_001369291.1:p.Gly493=
NM_001382363.1:c.926G= NP_001369292.1:p.Gly309=
NM_001382364.1:c.938G= NP_001369293.1:p.Gly313=
NM_001382448.1:c.1466G= NP_001369377.1:p.Gly489=
NM_178443.3:c.1478G= NP_848537.1:p.Gly493=