Canonical Allele Identifier: CA1978643022
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64223187C= , CM000673.2:g.64223187C= GRCh38
NC_000011.9:g.63990659C= , CM000673.1:g.63990659C= GRCh37
NC_000011.8:g.63747235C= NCBI36
NG_016360.1:g.21508C= , LRG_180:g.21508C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1822C= ENSP00000279227.5:p.Gln608=
ENST00000540554.2:n.3334C=
ENST00000541252.2:c.1270C= ENSP00000438885.2:p.Gln424=
ENST00000544997.6:c.1810C= ENSP00000445778.2:p.Gln604=
ENST00000545896.2:c.374C= ENSP00000440209.2:p.Ala125=
ENST00000546255.2:n.2114C=
ENST00000698845.1:c.*1005C= ENSP00000513981.1:n.*1005C=
ENST00000698846.1:n.2056C=
ENST00000698847.1:c.*1215C= ENSP00000513982.1:n.*1215C=
ENST00000698850.1:n.3831C=
ENST00000698852.1:c.1810C= ENSP00000513984.1:p.Gln604=
ENST00000698853.1:c.*1039C= ENSP00000513985.1:n.*1039C=
ENST00000698854.1:c.*1140C= ENSP00000513986.1:n.*1140C=
ENST00000698855.1:n.3462C=
ENST00000698856.1:n.3156C=
ENST00000698859.1:n.2320C=
ENST00000698860.1:c.1822C= ENSP00000513988.1:p.Gln608=
ENST00000698861.1:c.1810C= ENSP00000513989.1:p.Gln604=
ENST00000698862.1:c.*1106C= ENSP00000513990.1:n.*1106C=
ENST00000698863.1:c.1810C= ENSP00000513991.1:p.Gln604=
ENST00000698864.1:n.2371C=
ENST00000698865.1:c.1831C= ENSP00000513992.1:p.Gln611=
ENST00000698866.1:c.*1598C= ENSP00000513993.1:n.*1598C=
ENST00000698867.1:n.5785C=
ENST00000698868.1:c.1675C= ENSP00000513994.1:p.Gln559=
ENST00000698869.1:c.1576C= ENSP00000513995.1:p.Gln526=
ENST00000698870.1:c.1810C= ENSP00000513996.1:p.Gln604=
ENST00000698871.1:n.2333C=
ENST00000698872.1:c.*599C= ENSP00000513997.1:n.*599C=
ENST00000698873.1:c.*1005C= ENSP00000513998.1:n.*1005C=
ENST00000698874.1:c.1270C= ENSP00000513999.1:p.Gln424=
ENST00000698875.1:n.1670C=
ENST00000698876.1:n.1858C=
ENST00000698877.1:n.1378C=
ENST00000698878.1:c.1804C= ENSP00000514000.1:p.Gln602=
ENST00000698880.1:c.1678C=
ENST00000345728.10:c.1810C= MANE Select ENSP00000339950.5:p.Gln604=
ENST00000279227.9:c.1822C= ENSP00000279227.5:p.Gln608=
ENST00000345728.9:c.1810C= ENSP00000339950.5:p.Gln604=
ENST00000545896.1:c.373C= ENSP00000440209.1:p.Gln125=
NM_031471.5:c.1810C= NP_113659.3:p.Gln604=
NM_178443.2:c.1822C= , LRG_180t1:c.1822C= NP_848537.1:p.Gln608=
XM_011545294.1:c.1822C= XP_011543596.1:p.Gln608=
XM_011545295.1:c.1282C= XP_011543597.1:p.Gln428=
XM_011545296.1:c.1282C= XP_011543598.1:p.Gln428=
XM_011545294.3:c.1822C= XP_011543596.1:p.Gln608=
XM_011545295.2:c.1282C= XP_011543597.1:p.Gln428=
XM_017018398.2:c.1810C= XP_016873887.1:p.Gln604=
XM_017018399.1:c.1270C= XP_016873888.1:p.Gln424=
NM_031471.6:c.1810C= MANE Select NP_113659.3:p.Gln604=
NM_001382361.1:c.1810C= NP_001369290.1:p.Gln604=
NM_001382362.1:c.1822C= NP_001369291.1:p.Gln608=
NM_001382363.1:c.1270C= NP_001369292.1:p.Gln424=
NM_001382364.1:c.1282C= NP_001369293.1:p.Gln428=
NM_001382448.1:c.1810C= NP_001369377.1:p.Gln604=
NM_178443.3:c.1822C= NP_848537.1:p.Gln608=