Canonical Allele Identifier: CA1978642736
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64223049T= , CM000673.2:g.64223049T= GRCh38
NC_000011.9:g.63990521T= , CM000673.1:g.63990521T= GRCh37
NC_000011.8:g.63747097T= NCBI36
NG_016360.1:g.21370T= , LRG_180:g.21370T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1684T= ENSP00000279227.5:p.Phe562=
ENST00000540554.2:n.3196T=
ENST00000541252.2:c.1132T= ENSP00000438885.2:p.Phe378=
ENST00000544997.6:c.1672T= ENSP00000445778.2:p.Phe558=
ENST00000545896.2:c.236T= ENSP00000440209.2:p.Val79=
ENST00000546255.2:n.1976T=
ENST00000698845.1:c.*867T= ENSP00000513981.1:n.*867T=
ENST00000698846.1:n.1918T=
ENST00000698847.1:c.*1077T= ENSP00000513982.1:n.*1077T=
ENST00000698850.1:n.3693T=
ENST00000698852.1:c.1672T= ENSP00000513984.1:p.Phe558=
ENST00000698853.1:c.*901T= ENSP00000513985.1:n.*901T=
ENST00000698854.1:c.*1002T= ENSP00000513986.1:n.*1002T=
ENST00000698855.1:n.3324T=
ENST00000698856.1:n.3018T=
ENST00000698859.1:n.2182T=
ENST00000698860.1:c.1684T= ENSP00000513988.1:p.Phe562=
ENST00000698861.1:c.1672T= ENSP00000513989.1:p.Phe558=
ENST00000698862.1:c.*968T= ENSP00000513990.1:n.*968T=
ENST00000698863.1:c.1672T= ENSP00000513991.1:p.Phe558=
ENST00000698864.1:n.2233T=
ENST00000698865.1:c.1693T= ENSP00000513992.1:p.Phe565=
ENST00000698866.1:c.*1460T= ENSP00000513993.1:n.*1460T=
ENST00000698867.1:n.5647T=
ENST00000698868.1:c.1537T= ENSP00000513994.1:p.Phe513=
ENST00000698869.1:c.1438T= ENSP00000513995.1:p.Phe480=
ENST00000698870.1:c.1672T= ENSP00000513996.1:p.Phe558=
ENST00000698871.1:n.2195T=
ENST00000698872.1:c.*461T= ENSP00000513997.1:n.*461T=
ENST00000698873.1:c.*867T= ENSP00000513998.1:n.*867T=
ENST00000698874.1:c.1132T= ENSP00000513999.1:p.Phe378=
ENST00000698875.1:n.1532T=
ENST00000698876.1:n.1720T=
ENST00000698877.1:n.1240T=
ENST00000698878.1:c.1666T= ENSP00000514000.1:p.Phe556=
ENST00000698880.1:c.1540T=
ENST00000345728.10:c.1672T= MANE Select ENSP00000339950.5:p.Phe558=
ENST00000279227.9:c.1684T= ENSP00000279227.5:p.Phe562=
ENST00000345728.9:c.1672T= ENSP00000339950.5:p.Phe558=
ENST00000540554.1:n.308T=
ENST00000545896.1:c.235T= ENSP00000440209.1:p.Phe79=
NM_031471.5:c.1672T= NP_113659.3:p.Phe558=
NM_178443.2:c.1684T= , LRG_180t1:c.1684T= NP_848537.1:p.Phe562=
XM_011545294.1:c.1684T= XP_011543596.1:p.Phe562=
XM_011545295.1:c.1144T= XP_011543597.1:p.Phe382=
XM_011545296.1:c.1144T= XP_011543598.1:p.Phe382=
XM_011545294.3:c.1684T= XP_011543596.1:p.Phe562=
XM_011545295.2:c.1144T= XP_011543597.1:p.Phe382=
XM_017018398.2:c.1672T= XP_016873887.1:p.Phe558=
XM_017018399.1:c.1132T= XP_016873888.1:p.Phe378=
NM_031471.6:c.1672T= MANE Select NP_113659.3:p.Phe558=
NM_001382361.1:c.1672T= NP_001369290.1:p.Phe558=
NM_001382362.1:c.1684T= NP_001369291.1:p.Phe562=
NM_001382363.1:c.1132T= NP_001369292.1:p.Phe378=
NM_001382364.1:c.1144T= NP_001369293.1:p.Phe382=
NM_001382448.1:c.1672T= NP_001369377.1:p.Phe558=
NM_178443.3:c.1684T= NP_848537.1:p.Phe562=