Canonical Allele Identifier: CA1978638387
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220187C= , CM000673.2:g.64220187C= GRCh38
NC_000011.9:g.63987659C= , CM000673.1:g.63987659C= GRCh37
NC_000011.8:g.63744235C= NCBI36
NG_016360.1:g.18508C= , LRG_180:g.18508C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1217-33C= ENSP00000279227.5:n.1217-33C=
ENST00000540554.2:n.2274-33C=
ENST00000541252.2:c.665-33C= ENSP00000438885.2:n.665-33C=
ENST00000541326.6:n.517-33C=
ENST00000544997.6:c.1205-33C= ENSP00000445778.2:n.1205-33C=
ENST00000546255.2:n.1400-33C=
ENST00000698845.1:c.*400-33C= ENSP00000513981.1:n.*400-33C=
ENST00000698846.1:n.1342-33C=
ENST00000698847.1:c.*610-33C= ENSP00000513982.1:n.*610-33C=
ENST00000698848.1:n.394-33C=
ENST00000698849.1:n.325-33C=
ENST00000698850.1:n.864-33C=
ENST00000698852.1:c.1205-33C= ENSP00000513984.1:n.1205-33C=
ENST00000698853.1:c.*434-33C= ENSP00000513985.1:n.*434-33C=
ENST00000698854.1:c.*535-33C= ENSP00000513986.1:n.*535-33C=
ENST00000698855.1:n.2857-33C=
ENST00000698856.1:n.2442-33C=
ENST00000698859.1:n.1369-33C=
ENST00000698860.1:c.1217-33C= ENSP00000513988.1:n.1217-33C=
ENST00000698861.1:c.1205-33C= ENSP00000513989.1:n.1205-33C=
ENST00000698862.1:c.*501-33C= ENSP00000513990.1:n.*501-33C=
ENST00000698863.1:c.1205-33C= ENSP00000513991.1:n.1205-33C=
ENST00000698864.1:n.1311-33C=
ENST00000698865.1:c.1226-33C= ENSP00000513992.1:n.1226-33C=
ENST00000698866.1:c.*610-33C= ENSP00000513993.1:n.*610-33C=
ENST00000698867.1:n.5180-33C=
ENST00000698868.1:c.1070-33C= ENSP00000513994.1:n.1070-33C=
ENST00000698869.1:c.1205-33C= ENSP00000513995.1:n.1205-33C=
ENST00000698870.1:c.1205-33C= ENSP00000513996.1:n.1205-33C=
ENST00000698871.1:n.1728-33C=
ENST00000698872.1:c.660-33C= ENSP00000513997.1:n.660-33C=
ENST00000698873.1:c.*400-33C= ENSP00000513998.1:n.*400-33C=
ENST00000698874.1:c.665-33C= ENSP00000513999.1:n.665-33C=
ENST00000698875.1:n.1065-33C=
ENST00000698876.1:n.1144-33C=
ENST00000698877.1:n.773-33C=
ENST00000698878.1:c.1205-33C= ENSP00000514000.1:n.1205-33C=
ENST00000698880.1:c.1045-33C=
ENST00000345728.10:c.1205-33C= MANE Select ENSP00000339950.5:n.1205-33C=
ENST00000279227.9:c.1217-33C= ENSP00000279227.5:n.1217-33C=
ENST00000345728.9:c.1205-33C= ENSP00000339950.5:n.1205-33C=
ENST00000540957.1:n.358-33C=
ENST00000541326.5:n.512-33C=
NM_031471.5:c.1205-33C= NP_113659.3:n.1205-33C=
NM_178443.2:c.1217-33C= , LRG_180t1:c.1217-33C= NP_848537.1:n.1217-33C=
XM_011545294.1:c.1217-33C= XP_011543596.1:n.1217-33C=
XM_011545295.1:c.677-33C= XP_011543597.1:n.677-33C=
XM_011545296.1:c.677-33C= XP_011543598.1:n.677-33C=
XM_011545294.3:c.1217-33C= XP_011543596.1:n.1217-33C=
XM_011545295.2:c.677-33C= XP_011543597.1:n.677-33C=
XM_017018398.2:c.1205-33C= XP_016873887.1:n.1205-33C=
XM_017018399.1:c.665-33C= XP_016873888.1:n.665-33C=
NM_031471.6:c.1205-33C= MANE Select NP_113659.3:n.1205-33C=
NM_001382361.1:c.1205-33C= NP_001369290.1:n.1205-33C=
NM_001382362.1:c.1217-33C= NP_001369291.1:n.1217-33C=
NM_001382363.1:c.665-33C= NP_001369292.1:n.665-33C=
NM_001382364.1:c.677-33C= NP_001369293.1:n.677-33C=
NM_001382448.1:c.1205-33C= NP_001369377.1:n.1205-33C=
NM_178443.3:c.1217-33C= NP_848537.1:n.1217-33C=