Canonical Allele Identifier: CA2840550024
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220464dup , CM000673.2:g.64220464dup GRCh38
NC_000011.9:g.63987936dup , CM000673.1:g.63987936dup GRCh37
NC_000011.8:g.63744512dup NCBI36
NG_016360.1:g.18785dup , LRG_180:g.18785dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1352dup ENSP00000279227.5:p.Cys452LeufsTer?
ENST00000540554.2:n.2518dup
ENST00000541252.2:c.800dup ENSP00000438885.2:p.Cys268LeufsTer?
ENST00000541326.6:n.761dup
ENST00000544997.6:c.1340dup ENSP00000445778.2:p.Cys448LeufsTer?
ENST00000545896.2:c.29dup ENSP00000440209.2:p.Cys11LeufsTer?
ENST00000546255.2:n.1644dup
ENST00000698845.1:c.*535dup ENSP00000513981.1:n.*535dup
ENST00000698846.1:n.1586dup
ENST00000698847.1:c.*745dup ENSP00000513982.1:n.*745dup
ENST00000698848.1:n.638dup
ENST00000698849.1:n.460dup
ENST00000698850.1:n.1108dup
ENST00000698852.1:c.1340dup ENSP00000513984.1:p.Cys448LeufsTer?
ENST00000698853.1:c.*569dup ENSP00000513985.1:n.*569dup
ENST00000698854.1:c.*670dup ENSP00000513986.1:n.*670dup
ENST00000698855.1:n.2992dup
ENST00000698856.1:n.2686dup
ENST00000698859.1:n.1504dup
ENST00000698860.1:c.1352dup ENSP00000513988.1:p.Cys452LeufsTer?
ENST00000698861.1:c.1340dup ENSP00000513989.1:p.Cys448LeufsTer?
ENST00000698862.1:c.*636dup ENSP00000513990.1:n.*636dup
ENST00000698863.1:c.1340dup ENSP00000513991.1:p.Cys448LeufsTer?
ENST00000698864.1:n.1555dup
ENST00000698865.1:c.1361dup ENSP00000513992.1:p.Cys455LeufsTer?
ENST00000698866.1:c.*854dup ENSP00000513993.1:n.*854dup
ENST00000698867.1:n.5315dup
ENST00000698868.1:c.1205dup ENSP00000513994.1:p.Cys403LeufsTer?
ENST00000698869.1:c.1311+138dup ENSP00000513995.1:n.1311+138dup
ENST00000698870.1:c.1340dup ENSP00000513996.1:p.Cys448LeufsTer?
ENST00000698871.1:n.1863dup
ENST00000698872.1:c.*129dup ENSP00000513997.1:n.*129dup
ENST00000698873.1:c.*535dup ENSP00000513998.1:n.*535dup
ENST00000698874.1:c.800dup ENSP00000513999.1:p.Cys268LeufsTer?
ENST00000698875.1:n.1200dup
ENST00000698876.1:n.1388dup
ENST00000698877.1:n.908dup
ENST00000698878.1:c.1334dup ENSP00000514000.1:p.Cys446LeufsTer?
ENST00000698880.1:c.1208dup
ENST00000345728.10:c.1340dup MANE Select ENSP00000339950.5:p.Cys448LeufsTer?
ENST00000279227.9:c.1352dup ENSP00000279227.5:p.Cys452LeufsTer?
ENST00000345728.9:c.1340dup ENSP00000339950.5:p.Cys448LeufsTer?
ENST00000541326.5:n.756dup
ENST00000545896.1:c.28dup ENSP00000440209.1:p.Ala10GlyfsTer?
NM_031471.5:c.1340dup NP_113659.3:p.Cys448LeufsTer?
NM_178443.2:c.1352dup , LRG_180t1:c.1352dup NP_848537.1:p.Cys452LeufsTer?
XM_011545294.1:c.1352dup XP_011543596.1:p.Cys452LeufsTer?
XM_011545295.1:c.812dup XP_011543597.1:p.Cys272LeufsTer?
XM_011545296.1:c.812dup XP_011543598.1:p.Cys272LeufsTer?
XM_011545294.3:c.1352dup XP_011543596.1:p.Cys452LeufsTer?
XM_011545295.2:c.812dup XP_011543597.1:p.Cys272LeufsTer?
XM_017018398.2:c.1340dup XP_016873887.1:p.Cys448LeufsTer?
XM_017018399.1:c.800dup XP_016873888.1:p.Cys268LeufsTer?
NM_031471.6:c.1340dup MANE Select NP_113659.3:p.Cys448LeufsTer?
NM_001382361.1:c.1340dup NP_001369290.1:p.Cys448LeufsTer?
NM_001382362.1:c.1352dup NP_001369291.1:p.Cys452LeufsTer?
NM_001382363.1:c.800dup NP_001369292.1:p.Cys268LeufsTer?
NM_001382364.1:c.812dup NP_001369293.1:p.Cys272LeufsTer?
NM_001382448.1:c.1340dup NP_001369377.1:p.Cys448LeufsTer?
NM_178443.3:c.1352dup NP_848537.1:p.Cys452LeufsTer?