Canonical Allele Identifier: CA1978639124
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220573G= , CM000673.2:g.64220573G= GRCh38
NC_000011.9:g.63988045G= , CM000673.1:g.63988045G= GRCh37
NC_000011.8:g.63744621G= NCBI36
NG_016360.1:g.18894G= , LRG_180:g.18894G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1461G= ENSP00000279227.5:p.Pro487=
ENST00000540554.2:n.2627G=
ENST00000541252.2:c.909G= ENSP00000438885.2:p.Pro303=
ENST00000541326.6:n.870G=
ENST00000544997.6:c.1449G= ENSP00000445778.2:p.Pro483=
ENST00000545896.2:c.138G= ENSP00000440209.2:p.Pro46=
ENST00000546255.2:n.1753G=
ENST00000698845.1:c.*644G= ENSP00000513981.1:n.*644G=
ENST00000698846.1:n.1695G=
ENST00000698847.1:c.*854G= ENSP00000513982.1:n.*854G=
ENST00000698849.1:n.569G=
ENST00000698850.1:n.1217G=
ENST00000698852.1:c.1449G= ENSP00000513984.1:p.Pro483=
ENST00000698853.1:c.*678G= ENSP00000513985.1:n.*678G=
ENST00000698854.1:c.*779G= ENSP00000513986.1:n.*779G=
ENST00000698855.1:n.3101G=
ENST00000698856.1:n.2795G=
ENST00000698859.1:n.1613G=
ENST00000698860.1:c.1461G= ENSP00000513988.1:p.Pro487=
ENST00000698861.1:c.1449G= ENSP00000513989.1:p.Pro483=
ENST00000698862.1:c.*745G= ENSP00000513990.1:n.*745G=
ENST00000698863.1:c.1449G= ENSP00000513991.1:p.Pro483=
ENST00000698864.1:n.1664G=
ENST00000698865.1:c.1470G= ENSP00000513992.1:p.Pro490=
ENST00000698866.1:c.*963G= ENSP00000513993.1:n.*963G=
ENST00000698867.1:n.5424G=
ENST00000698868.1:c.1314G= ENSP00000513994.1:p.Pro438=
ENST00000698869.1:c.1311+247G= ENSP00000513995.1:n.1311+247G=
ENST00000698870.1:c.1449G= ENSP00000513996.1:p.Pro483=
ENST00000698871.1:n.1972G=
ENST00000698872.1:c.*238G= ENSP00000513997.1:n.*238G=
ENST00000698873.1:c.*644G= ENSP00000513998.1:n.*644G=
ENST00000698874.1:c.909G= ENSP00000513999.1:p.Pro303=
ENST00000698875.1:n.1309G=
ENST00000698876.1:n.1497G=
ENST00000698877.1:n.1017G=
ENST00000698878.1:c.1443G= ENSP00000514000.1:p.Pro481=
ENST00000698880.1:c.1317G=
ENST00000345728.10:c.1449G= MANE Select ENSP00000339950.5:p.Pro483=
ENST00000279227.9:c.1461G= ENSP00000279227.5:p.Pro487=
ENST00000345728.9:c.1449G= ENSP00000339950.5:p.Pro483=
ENST00000541326.5:n.865G=
ENST00000545896.1:c.137G= ENSP00000440209.1:p.Arg46=
NM_031471.5:c.1449G= NP_113659.3:p.Pro483=
NM_178443.2:c.1461G= , LRG_180t1:c.1461G= NP_848537.1:p.Pro487=
XM_011545294.1:c.1461G= XP_011543596.1:p.Pro487=
XM_011545295.1:c.921G= XP_011543597.1:p.Pro307=
XM_011545296.1:c.921G= XP_011543598.1:p.Pro307=
XM_011545294.3:c.1461G= XP_011543596.1:p.Pro487=
XM_011545295.2:c.921G= XP_011543597.1:p.Pro307=
XM_017018398.2:c.1449G= XP_016873887.1:p.Pro483=
XM_017018399.1:c.909G= XP_016873888.1:p.Pro303=
NM_031471.6:c.1449G= MANE Select NP_113659.3:p.Pro483=
NM_001382361.1:c.1449G= NP_001369290.1:p.Pro483=
NM_001382362.1:c.1461G= NP_001369291.1:p.Pro487=
NM_001382363.1:c.909G= NP_001369292.1:p.Pro303=
NM_001382364.1:c.921G= NP_001369293.1:p.Pro307=
NM_001382448.1:c.1449G= NP_001369377.1:p.Pro483=
NM_178443.3:c.1461G= NP_848537.1:p.Pro487=