Canonical Allele Identifier: CA1978638900
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220476C= , CM000673.2:g.64220476C= GRCh38
NC_000011.9:g.63987948C= , CM000673.1:g.63987948C= GRCh37
NC_000011.8:g.63744524C= NCBI36
NG_016360.1:g.18797C= , LRG_180:g.18797C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1364C= ENSP00000279227.5:p.Ala455=
ENST00000540554.2:n.2530C=
ENST00000541252.2:c.812C= ENSP00000438885.2:p.Ala271=
ENST00000541326.6:n.773C=
ENST00000544997.6:c.1352C= ENSP00000445778.2:p.Ala451=
ENST00000545896.2:c.41C= ENSP00000440209.2:p.Ala14=
ENST00000546255.2:n.1656C=
ENST00000698845.1:c.*547C= ENSP00000513981.1:n.*547C=
ENST00000698846.1:n.1598C=
ENST00000698847.1:c.*757C= ENSP00000513982.1:n.*757C=
ENST00000698848.1:n.650C=
ENST00000698849.1:n.472C=
ENST00000698850.1:n.1120C=
ENST00000698852.1:c.1352C= ENSP00000513984.1:p.Ala451=
ENST00000698853.1:c.*581C= ENSP00000513985.1:n.*581C=
ENST00000698854.1:c.*682C= ENSP00000513986.1:n.*682C=
ENST00000698855.1:n.3004C=
ENST00000698856.1:n.2698C=
ENST00000698859.1:n.1516C=
ENST00000698860.1:c.1364C= ENSP00000513988.1:p.Ala455=
ENST00000698861.1:c.1352C= ENSP00000513989.1:p.Ala451=
ENST00000698862.1:c.*648C= ENSP00000513990.1:n.*648C=
ENST00000698863.1:c.1352C= ENSP00000513991.1:p.Ala451=
ENST00000698864.1:n.1567C=
ENST00000698865.1:c.1373C= ENSP00000513992.1:p.Ala458=
ENST00000698866.1:c.*866C= ENSP00000513993.1:n.*866C=
ENST00000698867.1:n.5327C=
ENST00000698868.1:c.1217C= ENSP00000513994.1:p.Ala406=
ENST00000698869.1:c.1311+150C= ENSP00000513995.1:n.1311+150C=
ENST00000698870.1:c.1352C= ENSP00000513996.1:p.Ala451=
ENST00000698871.1:n.1875C=
ENST00000698872.1:c.*141C= ENSP00000513997.1:n.*141C=
ENST00000698873.1:c.*547C= ENSP00000513998.1:n.*547C=
ENST00000698874.1:c.812C= ENSP00000513999.1:p.Ala271=
ENST00000698875.1:n.1212C=
ENST00000698876.1:n.1400C=
ENST00000698877.1:n.920C=
ENST00000698878.1:c.1346C= ENSP00000514000.1:p.Ala449=
ENST00000698880.1:c.1220C=
ENST00000345728.10:c.1352C= MANE Select ENSP00000339950.5:p.Ala451=
ENST00000279227.9:c.1364C= ENSP00000279227.5:p.Ala455=
ENST00000345728.9:c.1352C= ENSP00000339950.5:p.Ala451=
ENST00000541326.5:n.768C=
ENST00000545896.1:c.40C= ENSP00000440209.1:p.Pro14=
NM_031471.5:c.1352C= NP_113659.3:p.Ala451=
NM_178443.2:c.1364C= , LRG_180t1:c.1364C= NP_848537.1:p.Ala455=
XM_011545294.1:c.1364C= XP_011543596.1:p.Ala455=
XM_011545295.1:c.824C= XP_011543597.1:p.Ala275=
XM_011545296.1:c.824C= XP_011543598.1:p.Ala275=
XM_011545294.3:c.1364C= XP_011543596.1:p.Ala455=
XM_011545295.2:c.824C= XP_011543597.1:p.Ala275=
XM_017018398.2:c.1352C= XP_016873887.1:p.Ala451=
XM_017018399.1:c.812C= XP_016873888.1:p.Ala271=
NM_031471.6:c.1352C= MANE Select NP_113659.3:p.Ala451=
NM_001382361.1:c.1352C= NP_001369290.1:p.Ala451=
NM_001382362.1:c.1364C= NP_001369291.1:p.Ala455=
NM_001382363.1:c.812C= NP_001369292.1:p.Ala271=
NM_001382364.1:c.824C= NP_001369293.1:p.Ala275=
NM_001382448.1:c.1352C= NP_001369377.1:p.Ala451=
NM_178443.3:c.1364C= NP_848537.1:p.Ala455=