Canonical Allele Identifier: CA2574859443

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223184del , CM000673.2:g.64223184del	GRCh38
NC_000011.9:g.63990656del , CM000673.1:g.63990656del	GRCh37
NC_000011.8:g.63747232del	NCBI36
NG_016360.1:g.21505del , LRG_180:g.21505del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1819del	ENSP00000279227.5:p.Arg607GlyfsTer?
ENST00000540554.2:n.3331del
ENST00000541252.2:c.1267del	ENSP00000438885.2:p.Arg423GlyfsTer?
ENST00000544997.6:c.1807del	ENSP00000445778.2:p.Arg603GlyfsTer?
ENST00000545896.2:c.371del	ENSP00000440209.2:p.Pro124ArgfsTer?
ENST00000546255.2:n.2111del
ENST00000698845.1:c.*1002del	ENSP00000513981.1:n.*1002del
ENST00000698846.1:n.2053del
ENST00000698847.1:c.*1212del	ENSP00000513982.1:n.*1212del
ENST00000698850.1:n.3828del
ENST00000698852.1:c.1807del	ENSP00000513984.1:p.Arg603GlyfsTer?
ENST00000698853.1:c.*1036del	ENSP00000513985.1:n.*1036del
ENST00000698854.1:c.*1137del	ENSP00000513986.1:n.*1137del
ENST00000698855.1:n.3459del
ENST00000698856.1:n.3153del
ENST00000698859.1:n.2317del
ENST00000698860.1:c.1819del	ENSP00000513988.1:p.Arg607GlyfsTer?
ENST00000698861.1:c.1807del	ENSP00000513989.1:p.Arg603GlyfsTer?
ENST00000698862.1:c.*1103del	ENSP00000513990.1:n.*1103del
ENST00000698863.1:c.1807del	ENSP00000513991.1:p.Arg603GlyfsTer?
ENST00000698864.1:n.2368del
ENST00000698865.1:c.1828del	ENSP00000513992.1:p.Arg610GlyfsTer?
ENST00000698866.1:c.*1595del	ENSP00000513993.1:n.*1595del
ENST00000698867.1:n.5782del
ENST00000698868.1:c.1672del	ENSP00000513994.1:p.Arg558GlyfsTer?
ENST00000698869.1:c.1573del	ENSP00000513995.1:p.Arg525GlyfsTer?
ENST00000698870.1:c.1807del	ENSP00000513996.1:p.Arg603GlyfsTer?
ENST00000698871.1:n.2330del
ENST00000698872.1:c.*596del	ENSP00000513997.1:n.*596del
ENST00000698873.1:c.*1002del	ENSP00000513998.1:n.*1002del
ENST00000698874.1:c.1267del	ENSP00000513999.1:p.Arg423GlyfsTer?
ENST00000698875.1:n.1667del
ENST00000698876.1:n.1855del
ENST00000698877.1:n.1375del
ENST00000698878.1:c.1801del	ENSP00000514000.1:p.Arg601GlyfsTer?
ENST00000698880.1:c.1675del
ENST00000345728.10:c.1807del MANE Select	ENSP00000339950.5:p.Arg603GlyfsTer?
ENST00000279227.9:c.1819del	ENSP00000279227.5:p.Arg607GlyfsTer?
ENST00000345728.9:c.1807del	ENSP00000339950.5:p.Arg603GlyfsTer?
ENST00000545896.1:c.370del	ENSP00000440209.1:p.Arg124GlyfsTer?
NM_031471.5:c.1807del	NP_113659.3:p.Arg603GlyfsTer?
NM_178443.2:c.1819del , LRG_180t1:c.1819del	NP_848537.1:p.Arg607GlyfsTer?
XM_011545294.1:c.1819del	XP_011543596.1:p.Arg607GlyfsTer?
XM_011545295.1:c.1279del	XP_011543597.1:p.Arg427GlyfsTer?
XM_011545296.1:c.1279del	XP_011543598.1:p.Arg427GlyfsTer?
XM_011545294.3:c.1819del	XP_011543596.1:p.Arg607GlyfsTer?
XM_011545295.2:c.1279del	XP_011543597.1:p.Arg427GlyfsTer?
XM_017018398.2:c.1807del	XP_016873887.1:p.Arg603GlyfsTer?
XM_017018399.1:c.1267del	XP_016873888.1:p.Arg423GlyfsTer?
NM_031471.6:c.1807del MANE Select	NP_113659.3:p.Arg603GlyfsTer?
NM_001382361.1:c.1807del	NP_001369290.1:p.Arg603GlyfsTer?
NM_001382362.1:c.1819del	NP_001369291.1:p.Arg607GlyfsTer?
NM_001382363.1:c.1267del	NP_001369292.1:p.Arg423GlyfsTer?
NM_001382364.1:c.1279del	NP_001369293.1:p.Arg427GlyfsTer?
NM_001382448.1:c.1807del	NP_001369377.1:p.Arg603GlyfsTer?
NM_178443.3:c.1819del	NP_848537.1:p.Arg607GlyfsTer?