Canonical Allele Identifier: CA1978638521
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220246G= , CM000673.2:g.64220246G= GRCh38
NC_000011.9:g.63987718G= , CM000673.1:g.63987718G= GRCh37
NC_000011.8:g.63744294G= NCBI36
NG_016360.1:g.18567G= , LRG_180:g.18567G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1243G= ENSP00000279227.5:p.Val415=
ENST00000540554.2:n.2300G=
ENST00000541252.2:c.691G= ENSP00000438885.2:p.Val231=
ENST00000541326.6:n.543G=
ENST00000544997.6:c.1231G= ENSP00000445778.2:p.Val411=
ENST00000546255.2:n.1426G=
ENST00000698845.1:c.*426G= ENSP00000513981.1:n.*426G=
ENST00000698846.1:n.1368G=
ENST00000698847.1:c.*636G= ENSP00000513982.1:n.*636G=
ENST00000698848.1:n.420G=
ENST00000698849.1:n.351G=
ENST00000698850.1:n.890G=
ENST00000698852.1:c.1231G= ENSP00000513984.1:p.Val411=
ENST00000698853.1:c.*460G= ENSP00000513985.1:n.*460G=
ENST00000698854.1:c.*561G= ENSP00000513986.1:n.*561G=
ENST00000698855.1:n.2883G=
ENST00000698856.1:n.2468G=
ENST00000698859.1:n.1395G=
ENST00000698860.1:c.1243G= ENSP00000513988.1:p.Val415=
ENST00000698861.1:c.1231G= ENSP00000513989.1:p.Val411=
ENST00000698862.1:c.*527G= ENSP00000513990.1:n.*527G=
ENST00000698863.1:c.1231G= ENSP00000513991.1:p.Val411=
ENST00000698864.1:n.1337G=
ENST00000698865.1:c.1252G= ENSP00000513992.1:p.Val418=
ENST00000698866.1:c.*636G= ENSP00000513993.1:n.*636G=
ENST00000698867.1:n.5206G=
ENST00000698868.1:c.1096G= ENSP00000513994.1:p.Val366=
ENST00000698869.1:c.1231G= ENSP00000513995.1:p.Val411=
ENST00000698870.1:c.1231G= ENSP00000513996.1:p.Val411=
ENST00000698871.1:n.1754G=
ENST00000698872.1:c.*20G= ENSP00000513997.1:n.*20G=
ENST00000698873.1:c.*426G= ENSP00000513998.1:n.*426G=
ENST00000698874.1:c.691G= ENSP00000513999.1:p.Val231=
ENST00000698875.1:n.1091G=
ENST00000698876.1:n.1170G=
ENST00000698877.1:n.799G=
ENST00000698878.1:c.1231G= ENSP00000514000.1:p.Val411=
ENST00000698880.1:c.1071G=
ENST00000345728.10:c.1231G= MANE Select ENSP00000339950.5:p.Val411=
ENST00000279227.9:c.1243G= ENSP00000279227.5:p.Val415=
ENST00000345728.9:c.1231G= ENSP00000339950.5:p.Val411=
ENST00000540957.1:n.384G=
ENST00000541326.5:n.538G=
NM_031471.5:c.1231G= NP_113659.3:p.Val411=
NM_178443.2:c.1243G= , LRG_180t1:c.1243G= NP_848537.1:p.Val415=
XM_011545294.1:c.1243G= XP_011543596.1:p.Val415=
XM_011545295.1:c.703G= XP_011543597.1:p.Val235=
XM_011545296.1:c.703G= XP_011543598.1:p.Val235=
XM_011545294.3:c.1243G= XP_011543596.1:p.Val415=
XM_011545295.2:c.703G= XP_011543597.1:p.Val235=
XM_017018398.2:c.1231G= XP_016873887.1:p.Val411=
XM_017018399.1:c.691G= XP_016873888.1:p.Val231=
NM_031471.6:c.1231G= MANE Select NP_113659.3:p.Val411=
NM_001382361.1:c.1231G= NP_001369290.1:p.Val411=
NM_001382362.1:c.1243G= NP_001369291.1:p.Val415=
NM_001382363.1:c.691G= NP_001369292.1:p.Val231=
NM_001382364.1:c.703G= NP_001369293.1:p.Val235=
NM_001382448.1:c.1231G= NP_001369377.1:p.Val411=
NM_178443.3:c.1243G= NP_848537.1:p.Val415=