Canonical Allele Identifier: CA1978639057
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220548T= , CM000673.2:g.64220548T= GRCh38
NC_000011.9:g.63988020T= , CM000673.1:g.63988020T= GRCh37
NC_000011.8:g.63744596T= NCBI36
NG_016360.1:g.18869T= , LRG_180:g.18869T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1436T= ENSP00000279227.5:p.Leu479=
ENST00000540554.2:n.2602T=
ENST00000541252.2:c.884T= ENSP00000438885.2:p.Leu295=
ENST00000541326.6:n.845T=
ENST00000544997.6:c.1424T= ENSP00000445778.2:p.Leu475=
ENST00000545896.2:c.113T= ENSP00000440209.2:p.Leu38=
ENST00000546255.2:n.1728T=
ENST00000698845.1:c.*619T= ENSP00000513981.1:n.*619T=
ENST00000698846.1:n.1670T=
ENST00000698847.1:c.*829T= ENSP00000513982.1:n.*829T=
ENST00000698849.1:n.544T=
ENST00000698850.1:n.1192T=
ENST00000698852.1:c.1424T= ENSP00000513984.1:p.Leu475=
ENST00000698853.1:c.*653T= ENSP00000513985.1:n.*653T=
ENST00000698854.1:c.*754T= ENSP00000513986.1:n.*754T=
ENST00000698855.1:n.3076T=
ENST00000698856.1:n.2770T=
ENST00000698859.1:n.1588T=
ENST00000698860.1:c.1436T= ENSP00000513988.1:p.Leu479=
ENST00000698861.1:c.1424T= ENSP00000513989.1:p.Leu475=
ENST00000698862.1:c.*720T= ENSP00000513990.1:n.*720T=
ENST00000698863.1:c.1424T= ENSP00000513991.1:p.Leu475=
ENST00000698864.1:n.1639T=
ENST00000698865.1:c.1445T= ENSP00000513992.1:p.Leu482=
ENST00000698866.1:c.*938T= ENSP00000513993.1:n.*938T=
ENST00000698867.1:n.5399T=
ENST00000698868.1:c.1289T= ENSP00000513994.1:p.Leu430=
ENST00000698869.1:c.1311+222T= ENSP00000513995.1:n.1311+222T=
ENST00000698870.1:c.1424T= ENSP00000513996.1:p.Leu475=
ENST00000698871.1:n.1947T=
ENST00000698872.1:c.*213T= ENSP00000513997.1:n.*213T=
ENST00000698873.1:c.*619T= ENSP00000513998.1:n.*619T=
ENST00000698874.1:c.884T= ENSP00000513999.1:p.Leu295=
ENST00000698875.1:n.1284T=
ENST00000698876.1:n.1472T=
ENST00000698877.1:n.992T=
ENST00000698878.1:c.1418T= ENSP00000514000.1:p.Leu473=
ENST00000698880.1:c.1292T=
ENST00000345728.10:c.1424T= MANE Select ENSP00000339950.5:p.Leu475=
ENST00000279227.9:c.1436T= ENSP00000279227.5:p.Leu479=
ENST00000345728.9:c.1424T= ENSP00000339950.5:p.Leu475=
ENST00000541326.5:n.840T=
ENST00000545896.1:c.112T= ENSP00000440209.1:p.Cys38=
NM_031471.5:c.1424T= NP_113659.3:p.Leu475=
NM_178443.2:c.1436T= , LRG_180t1:c.1436T= NP_848537.1:p.Leu479=
XM_011545294.1:c.1436T= XP_011543596.1:p.Leu479=
XM_011545295.1:c.896T= XP_011543597.1:p.Leu299=
XM_011545296.1:c.896T= XP_011543598.1:p.Leu299=
XM_011545294.3:c.1436T= XP_011543596.1:p.Leu479=
XM_011545295.2:c.896T= XP_011543597.1:p.Leu299=
XM_017018398.2:c.1424T= XP_016873887.1:p.Leu475=
XM_017018399.1:c.884T= XP_016873888.1:p.Leu295=
NM_031471.6:c.1424T= MANE Select NP_113659.3:p.Leu475=
NM_001382361.1:c.1424T= NP_001369290.1:p.Leu475=
NM_001382362.1:c.1436T= NP_001369291.1:p.Leu479=
NM_001382363.1:c.884T= NP_001369292.1:p.Leu295=
NM_001382364.1:c.896T= NP_001369293.1:p.Leu299=
NM_001382448.1:c.1424T= NP_001369377.1:p.Leu475=
NM_178443.3:c.1436T= NP_848537.1:p.Leu479=