Canonical Allele Identifier: CA1978639206
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220624C= , CM000673.2:g.64220624C= GRCh38
NC_000011.9:g.63988096C= , CM000673.1:g.63988096C= GRCh37
NC_000011.8:g.63744672C= NCBI36
NG_016360.1:g.18945C= , LRG_180:g.18945C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1512C= ENSP00000279227.5:p.Tyr504=
ENST00000540554.2:n.2678C=
ENST00000541252.2:c.960C= ENSP00000438885.2:p.Tyr320=
ENST00000541326.6:n.921C=
ENST00000544997.6:c.1500C= ENSP00000445778.2:p.Tyr500=
ENST00000545896.2:c.189C= ENSP00000440209.2:p.Tyr63=
ENST00000546255.2:n.1804C=
ENST00000698845.1:c.*695C= ENSP00000513981.1:n.*695C=
ENST00000698846.1:n.1746C=
ENST00000698847.1:c.*905C= ENSP00000513982.1:n.*905C=
ENST00000698849.1:n.620C=
ENST00000698850.1:n.1268C=
ENST00000698852.1:c.1500C= ENSP00000513984.1:p.Tyr500=
ENST00000698853.1:c.*729C= ENSP00000513985.1:n.*729C=
ENST00000698854.1:c.*830C= ENSP00000513986.1:n.*830C=
ENST00000698855.1:n.3152C=
ENST00000698856.1:n.2846C=
ENST00000698859.1:n.1664C=
ENST00000698860.1:c.1512C= ENSP00000513988.1:p.Tyr504=
ENST00000698861.1:c.1500C= ENSP00000513989.1:p.Tyr500=
ENST00000698862.1:c.*796C= ENSP00000513990.1:n.*796C=
ENST00000698863.1:c.1500C= ENSP00000513991.1:p.Tyr500=
ENST00000698864.1:n.1715C=
ENST00000698865.1:c.1521C= ENSP00000513992.1:p.Tyr507=
ENST00000698866.1:c.*1014C= ENSP00000513993.1:n.*1014C=
ENST00000698867.1:n.5475C=
ENST00000698868.1:c.1365C= ENSP00000513994.1:p.Tyr455=
ENST00000698869.1:c.1311+298C= ENSP00000513995.1:n.1311+298C=
ENST00000698870.1:c.1500C= ENSP00000513996.1:p.Tyr500=
ENST00000698871.1:n.2023C=
ENST00000698872.1:c.*289C= ENSP00000513997.1:n.*289C=
ENST00000698873.1:c.*695C= ENSP00000513998.1:n.*695C=
ENST00000698874.1:c.960C= ENSP00000513999.1:p.Tyr320=
ENST00000698875.1:n.1360C=
ENST00000698876.1:n.1548C=
ENST00000698877.1:n.1068C=
ENST00000698878.1:c.1494C= ENSP00000514000.1:p.Tyr498=
ENST00000698880.1:c.1368C=
ENST00000345728.10:c.1500C= MANE Select ENSP00000339950.5:p.Tyr500=
ENST00000279227.9:c.1512C= ENSP00000279227.5:p.Tyr504=
ENST00000345728.9:c.1500C= ENSP00000339950.5:p.Tyr500=
ENST00000545896.1:c.188C= ENSP00000440209.1:p.Thr63=
NM_031471.5:c.1500C= NP_113659.3:p.Tyr500=
NM_178443.2:c.1512C= , LRG_180t1:c.1512C= NP_848537.1:p.Tyr504=
XM_011545294.1:c.1512C= XP_011543596.1:p.Tyr504=
XM_011545295.1:c.972C= XP_011543597.1:p.Tyr324=
XM_011545296.1:c.972C= XP_011543598.1:p.Tyr324=
XM_011545294.3:c.1512C= XP_011543596.1:p.Tyr504=
XM_011545295.2:c.972C= XP_011543597.1:p.Tyr324=
XM_017018398.2:c.1500C= XP_016873887.1:p.Tyr500=
XM_017018399.1:c.960C= XP_016873888.1:p.Tyr320=
NM_031471.6:c.1500C= MANE Select NP_113659.3:p.Tyr500=
NM_001382361.1:c.1500C= NP_001369290.1:p.Tyr500=
NM_001382362.1:c.1512C= NP_001369291.1:p.Tyr504=
NM_001382363.1:c.960C= NP_001369292.1:p.Tyr320=
NM_001382364.1:c.972C= NP_001369293.1:p.Tyr324=
NM_001382448.1:c.1500C= NP_001369377.1:p.Tyr500=
NM_178443.3:c.1512C= NP_848537.1:p.Tyr504=