Canonical Allele Identifier: CA1978642946
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64223135G= , CM000673.2:g.64223135G= GRCh38
NC_000011.9:g.63990607G= , CM000673.1:g.63990607G= GRCh37
NC_000011.8:g.63747183G= NCBI36
NG_016360.1:g.21456G= , LRG_180:g.21456G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1770G= ENSP00000279227.5:p.Lys590=
ENST00000540554.2:n.3282G=
ENST00000541252.2:c.1218G= ENSP00000438885.2:p.Lys406=
ENST00000544997.6:c.1758G= ENSP00000445778.2:p.Lys586=
ENST00000545896.2:c.322G= ENSP00000440209.2:p.Asp108=
ENST00000546255.2:n.2062G=
ENST00000698845.1:c.*953G= ENSP00000513981.1:n.*953G=
ENST00000698846.1:n.2004G=
ENST00000698847.1:c.*1163G= ENSP00000513982.1:n.*1163G=
ENST00000698850.1:n.3779G=
ENST00000698852.1:c.1758G= ENSP00000513984.1:p.Lys586=
ENST00000698853.1:c.*987G= ENSP00000513985.1:n.*987G=
ENST00000698854.1:c.*1088G= ENSP00000513986.1:n.*1088G=
ENST00000698855.1:n.3410G=
ENST00000698856.1:n.3104G=
ENST00000698859.1:n.2268G=
ENST00000698860.1:c.1770G= ENSP00000513988.1:p.Lys590=
ENST00000698861.1:c.1758G= ENSP00000513989.1:p.Lys586=
ENST00000698862.1:c.*1054G= ENSP00000513990.1:n.*1054G=
ENST00000698863.1:c.1758G= ENSP00000513991.1:p.Lys586=
ENST00000698864.1:n.2319G=
ENST00000698865.1:c.1779G= ENSP00000513992.1:p.Lys593=
ENST00000698866.1:c.*1546G= ENSP00000513993.1:n.*1546G=
ENST00000698867.1:n.5733G=
ENST00000698868.1:c.1623G= ENSP00000513994.1:p.Lys541=
ENST00000698869.1:c.1524G= ENSP00000513995.1:p.Lys508=
ENST00000698870.1:c.1758G= ENSP00000513996.1:p.Lys586=
ENST00000698871.1:n.2281G=
ENST00000698872.1:c.*547G= ENSP00000513997.1:n.*547G=
ENST00000698873.1:c.*953G= ENSP00000513998.1:n.*953G=
ENST00000698874.1:c.1218G= ENSP00000513999.1:p.Lys406=
ENST00000698875.1:n.1618G=
ENST00000698876.1:n.1806G=
ENST00000698877.1:n.1326G=
ENST00000698878.1:c.1752G= ENSP00000514000.1:p.Lys584=
ENST00000698880.1:c.1626G=
ENST00000345728.10:c.1758G= MANE Select ENSP00000339950.5:p.Lys586=
ENST00000279227.9:c.1770G= ENSP00000279227.5:p.Lys590=
ENST00000345728.9:c.1758G= ENSP00000339950.5:p.Lys586=
ENST00000545896.1:c.321G= ENSP00000440209.1:p.Lys107=
NM_031471.5:c.1758G= NP_113659.3:p.Lys586=
NM_178443.2:c.1770G= , LRG_180t1:c.1770G= NP_848537.1:p.Lys590=
XM_011545294.1:c.1770G= XP_011543596.1:p.Lys590=
XM_011545295.1:c.1230G= XP_011543597.1:p.Lys410=
XM_011545296.1:c.1230G= XP_011543598.1:p.Lys410=
XM_011545294.3:c.1770G= XP_011543596.1:p.Lys590=
XM_011545295.2:c.1230G= XP_011543597.1:p.Lys410=
XM_017018398.2:c.1758G= XP_016873887.1:p.Lys586=
XM_017018399.1:c.1218G= XP_016873888.1:p.Lys406=
NM_031471.6:c.1758G= MANE Select NP_113659.3:p.Lys586=
NM_001382361.1:c.1758G= NP_001369290.1:p.Lys586=
NM_001382362.1:c.1770G= NP_001369291.1:p.Lys590=
NM_001382363.1:c.1218G= NP_001369292.1:p.Lys406=
NM_001382364.1:c.1230G= NP_001369293.1:p.Lys410=
NM_001382448.1:c.1758G= NP_001369377.1:p.Lys586=
NM_178443.3:c.1770G= NP_848537.1:p.Lys590=