Canonical Allele Identifier: CA1978638837
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220439C= , CM000673.2:g.64220439C= GRCh38
NC_000011.9:g.63987911C= , CM000673.1:g.63987911C= GRCh37
NC_000011.8:g.63744487C= NCBI36
NG_016360.1:g.18760C= , LRG_180:g.18760C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1327C= ENSP00000279227.5:p.Gln443=
ENST00000540554.2:n.2493C=
ENST00000541252.2:c.775C= ENSP00000438885.2:p.Gln259=
ENST00000541326.6:n.736C=
ENST00000544997.6:c.1315C= ENSP00000445778.2:p.Gln439=
ENST00000545896.2:c.4C= ENSP00000440209.2:p.Gln2=
ENST00000546255.2:n.1619C=
ENST00000698845.1:c.*510C= ENSP00000513981.1:n.*510C=
ENST00000698846.1:n.1561C=
ENST00000698847.1:c.*720C= ENSP00000513982.1:n.*720C=
ENST00000698848.1:n.613C=
ENST00000698849.1:n.435C=
ENST00000698850.1:n.1083C=
ENST00000698852.1:c.1315C= ENSP00000513984.1:p.Gln439=
ENST00000698853.1:c.*544C= ENSP00000513985.1:n.*544C=
ENST00000698854.1:c.*645C= ENSP00000513986.1:n.*645C=
ENST00000698855.1:n.2967C=
ENST00000698856.1:n.2661C=
ENST00000698859.1:n.1479C=
ENST00000698860.1:c.1327C= ENSP00000513988.1:p.Gln443=
ENST00000698861.1:c.1315C= ENSP00000513989.1:p.Gln439=
ENST00000698862.1:c.*611C= ENSP00000513990.1:n.*611C=
ENST00000698863.1:c.1315C= ENSP00000513991.1:p.Gln439=
ENST00000698864.1:n.1530C=
ENST00000698865.1:c.1336C= ENSP00000513992.1:p.Gln446=
ENST00000698866.1:c.*829C= ENSP00000513993.1:n.*829C=
ENST00000698867.1:n.5290C=
ENST00000698868.1:c.1180C= ENSP00000513994.1:p.Gln394=
ENST00000698869.1:c.1311+113C= ENSP00000513995.1:n.1311+113C=
ENST00000698870.1:c.1315C= ENSP00000513996.1:p.Gln439=
ENST00000698871.1:n.1838C=
ENST00000698872.1:c.*104C= ENSP00000513997.1:n.*104C=
ENST00000698873.1:c.*510C= ENSP00000513998.1:n.*510C=
ENST00000698874.1:c.775C= ENSP00000513999.1:p.Gln259=
ENST00000698875.1:n.1175C=
ENST00000698876.1:n.1363C=
ENST00000698877.1:n.883C=
ENST00000698878.1:c.1312-3C= ENSP00000514000.1:n.1312-3C=
ENST00000698880.1:c.1183C=
ENST00000345728.10:c.1315C= MANE Select ENSP00000339950.5:p.Gln439=
ENST00000279227.9:c.1327C= ENSP00000279227.5:p.Gln443=
ENST00000345728.9:c.1315C= ENSP00000339950.5:p.Gln439=
ENST00000540957.1:n.577C=
ENST00000541326.5:n.731C=
ENST00000545896.1:c.3C= ENSP00000440209.1:p.Ser1=
NM_031471.5:c.1315C= NP_113659.3:p.Gln439=
NM_178443.2:c.1327C= , LRG_180t1:c.1327C= NP_848537.1:p.Gln443=
XM_011545294.1:c.1327C= XP_011543596.1:p.Gln443=
XM_011545295.1:c.787C= XP_011543597.1:p.Gln263=
XM_011545296.1:c.787C= XP_011543598.1:p.Gln263=
XM_011545294.3:c.1327C= XP_011543596.1:p.Gln443=
XM_011545295.2:c.787C= XP_011543597.1:p.Gln263=
XM_017018398.2:c.1315C= XP_016873887.1:p.Gln439=
XM_017018399.1:c.775C= XP_016873888.1:p.Gln259=
NM_031471.6:c.1315C= MANE Select NP_113659.3:p.Gln439=
NM_001382361.1:c.1315C= NP_001369290.1:p.Gln439=
NM_001382362.1:c.1327C= NP_001369291.1:p.Gln443=
NM_001382363.1:c.775C= NP_001369292.1:p.Gln259=
NM_001382364.1:c.787C= NP_001369293.1:p.Gln263=
NM_001382448.1:c.1315C= NP_001369377.1:p.Gln439=
NM_178443.3:c.1327C= NP_848537.1:p.Gln443=