Canonical Allele Identifier: CA1978638477
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220228G= , CM000673.2:g.64220228G= GRCh38
NC_000011.9:g.63987700G= , CM000673.1:g.63987700G= GRCh37
NC_000011.8:g.63744276G= NCBI36
NG_016360.1:g.18549G= , LRG_180:g.18549G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1225G= ENSP00000279227.5:p.Val409=
ENST00000540554.2:n.2282G=
ENST00000541252.2:c.673G= ENSP00000438885.2:p.Val225=
ENST00000541326.6:n.525G=
ENST00000544997.6:c.1213G= ENSP00000445778.2:p.Val405=
ENST00000546255.2:n.1408G=
ENST00000698845.1:c.*408G= ENSP00000513981.1:n.*408G=
ENST00000698846.1:n.1350G=
ENST00000698847.1:c.*618G= ENSP00000513982.1:n.*618G=
ENST00000698848.1:n.402G=
ENST00000698849.1:n.333G=
ENST00000698850.1:n.872G=
ENST00000698852.1:c.1213G= ENSP00000513984.1:p.Val405=
ENST00000698853.1:c.*442G= ENSP00000513985.1:n.*442G=
ENST00000698854.1:c.*543G= ENSP00000513986.1:n.*543G=
ENST00000698855.1:n.2865G=
ENST00000698856.1:n.2450G=
ENST00000698859.1:n.1377G=
ENST00000698860.1:c.1225G= ENSP00000513988.1:p.Val409=
ENST00000698861.1:c.1213G= ENSP00000513989.1:p.Val405=
ENST00000698862.1:c.*509G= ENSP00000513990.1:n.*509G=
ENST00000698863.1:c.1213G= ENSP00000513991.1:p.Val405=
ENST00000698864.1:n.1319G=
ENST00000698865.1:c.1234G= ENSP00000513992.1:p.Val412=
ENST00000698866.1:c.*618G= ENSP00000513993.1:n.*618G=
ENST00000698867.1:n.5188G=
ENST00000698868.1:c.1078G= ENSP00000513994.1:p.Val360=
ENST00000698869.1:c.1213G= ENSP00000513995.1:p.Val405=
ENST00000698870.1:c.1213G= ENSP00000513996.1:p.Val405=
ENST00000698871.1:n.1736G=
ENST00000698872.1:c.*2G= ENSP00000513997.1:n.*2G=
ENST00000698873.1:c.*408G= ENSP00000513998.1:n.*408G=
ENST00000698874.1:c.673G= ENSP00000513999.1:p.Val225=
ENST00000698875.1:n.1073G=
ENST00000698876.1:n.1152G=
ENST00000698877.1:n.781G=
ENST00000698878.1:c.1213G= ENSP00000514000.1:p.Val405=
ENST00000698880.1:c.1053G=
ENST00000345728.10:c.1213G= MANE Select ENSP00000339950.5:p.Val405=
ENST00000279227.9:c.1225G= ENSP00000279227.5:p.Val409=
ENST00000345728.9:c.1213G= ENSP00000339950.5:p.Val405=
ENST00000540957.1:n.366G=
ENST00000541326.5:n.520G=
NM_031471.5:c.1213G= NP_113659.3:p.Val405=
NM_178443.2:c.1225G= , LRG_180t1:c.1225G= NP_848537.1:p.Val409=
XM_011545294.1:c.1225G= XP_011543596.1:p.Val409=
XM_011545295.1:c.685G= XP_011543597.1:p.Val229=
XM_011545296.1:c.685G= XP_011543598.1:p.Val229=
XM_011545294.3:c.1225G= XP_011543596.1:p.Val409=
XM_011545295.2:c.685G= XP_011543597.1:p.Val229=
XM_017018398.2:c.1213G= XP_016873887.1:p.Val405=
XM_017018399.1:c.673G= XP_016873888.1:p.Val225=
NM_031471.6:c.1213G= MANE Select NP_113659.3:p.Val405=
NM_001382361.1:c.1213G= NP_001369290.1:p.Val405=
NM_001382362.1:c.1225G= NP_001369291.1:p.Val409=
NM_001382363.1:c.673G= NP_001369292.1:p.Val225=
NM_001382364.1:c.685G= NP_001369293.1:p.Val229=
NM_001382448.1:c.1213G= NP_001369377.1:p.Val405=
NM_178443.3:c.1225G= NP_848537.1:p.Val409=