Canonical Allele Identifier: CA1978639109
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220565G= , CM000673.2:g.64220565G= GRCh38
NC_000011.9:g.63988037G= , CM000673.1:g.63988037G= GRCh37
NC_000011.8:g.63744613G= NCBI36
NG_016360.1:g.18886G= , LRG_180:g.18886G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1453G= ENSP00000279227.5:p.Gly485=
ENST00000540554.2:n.2619G=
ENST00000541252.2:c.901G= ENSP00000438885.2:p.Gly301=
ENST00000541326.6:n.862G=
ENST00000544997.6:c.1441G= ENSP00000445778.2:p.Gly481=
ENST00000545896.2:c.130G= ENSP00000440209.2:p.Gly44=
ENST00000546255.2:n.1745G=
ENST00000698845.1:c.*636G= ENSP00000513981.1:n.*636G=
ENST00000698846.1:n.1687G=
ENST00000698847.1:c.*846G= ENSP00000513982.1:n.*846G=
ENST00000698849.1:n.561G=
ENST00000698850.1:n.1209G=
ENST00000698852.1:c.1441G= ENSP00000513984.1:p.Gly481=
ENST00000698853.1:c.*670G= ENSP00000513985.1:n.*670G=
ENST00000698854.1:c.*771G= ENSP00000513986.1:n.*771G=
ENST00000698855.1:n.3093G=
ENST00000698856.1:n.2787G=
ENST00000698859.1:n.1605G=
ENST00000698860.1:c.1453G= ENSP00000513988.1:p.Gly485=
ENST00000698861.1:c.1441G= ENSP00000513989.1:p.Gly481=
ENST00000698862.1:c.*737G= ENSP00000513990.1:n.*737G=
ENST00000698863.1:c.1441G= ENSP00000513991.1:p.Gly481=
ENST00000698864.1:n.1656G=
ENST00000698865.1:c.1462G= ENSP00000513992.1:p.Gly488=
ENST00000698866.1:c.*955G= ENSP00000513993.1:n.*955G=
ENST00000698867.1:n.5416G=
ENST00000698868.1:c.1306G= ENSP00000513994.1:p.Gly436=
ENST00000698869.1:c.1311+239G= ENSP00000513995.1:n.1311+239G=
ENST00000698870.1:c.1441G= ENSP00000513996.1:p.Gly481=
ENST00000698871.1:n.1964G=
ENST00000698872.1:c.*230G= ENSP00000513997.1:n.*230G=
ENST00000698873.1:c.*636G= ENSP00000513998.1:n.*636G=
ENST00000698874.1:c.901G= ENSP00000513999.1:p.Gly301=
ENST00000698875.1:n.1301G=
ENST00000698876.1:n.1489G=
ENST00000698877.1:n.1009G=
ENST00000698878.1:c.1435G= ENSP00000514000.1:p.Gly479=
ENST00000698880.1:c.1309G=
ENST00000345728.10:c.1441G= MANE Select ENSP00000339950.5:p.Gly481=
ENST00000279227.9:c.1453G= ENSP00000279227.5:p.Gly485=
ENST00000345728.9:c.1441G= ENSP00000339950.5:p.Gly481=
ENST00000541326.5:n.857G=
ENST00000545896.1:c.129G= ENSP00000440209.1:p.Val43=
NM_031471.5:c.1441G= NP_113659.3:p.Gly481=
NM_178443.2:c.1453G= , LRG_180t1:c.1453G= NP_848537.1:p.Gly485=
XM_011545294.1:c.1453G= XP_011543596.1:p.Gly485=
XM_011545295.1:c.913G= XP_011543597.1:p.Gly305=
XM_011545296.1:c.913G= XP_011543598.1:p.Gly305=
XM_011545294.3:c.1453G= XP_011543596.1:p.Gly485=
XM_011545295.2:c.913G= XP_011543597.1:p.Gly305=
XM_017018398.2:c.1441G= XP_016873887.1:p.Gly481=
XM_017018399.1:c.901G= XP_016873888.1:p.Gly301=
NM_031471.6:c.1441G= MANE Select NP_113659.3:p.Gly481=
NM_001382361.1:c.1441G= NP_001369290.1:p.Gly481=
NM_001382362.1:c.1453G= NP_001369291.1:p.Gly485=
NM_001382363.1:c.901G= NP_001369292.1:p.Gly301=
NM_001382364.1:c.913G= NP_001369293.1:p.Gly305=
NM_001382448.1:c.1441G= NP_001369377.1:p.Gly481=
NM_178443.3:c.1453G= NP_848537.1:p.Gly485=