Canonical Allele Identifier: CA1978643006

Gene: FERMT3

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1819C=	ENSP00000279227.5:p.Arg607=
ENST00000540554.2:n.3331C=
ENST00000541252.2:c.1267C=	ENSP00000438885.2:p.Arg423=
ENST00000544997.6:c.1807C=	ENSP00000445778.2:p.Arg603=
ENST00000545896.2:c.371C=	ENSP00000440209.2:p.Pro124=
ENST00000546255.2:n.2111C=
ENST00000698845.1:c.*1002C=	ENSP00000513981.1:n.*1002C=
ENST00000698846.1:n.2053C=
ENST00000698847.1:c.*1212C=	ENSP00000513982.1:n.*1212C=
ENST00000698850.1:n.3828C=
ENST00000698852.1:c.1807C=	ENSP00000513984.1:p.Arg603=
ENST00000698853.1:c.*1036C=	ENSP00000513985.1:n.*1036C=
ENST00000698854.1:c.*1137C=	ENSP00000513986.1:n.*1137C=
ENST00000698855.1:n.3459C=
ENST00000698856.1:n.3153C=
ENST00000698859.1:n.2317C=
ENST00000698860.1:c.1819C=	ENSP00000513988.1:p.Arg607=
ENST00000698861.1:c.1807C=	ENSP00000513989.1:p.Arg603=
ENST00000698862.1:c.*1103C=	ENSP00000513990.1:n.*1103C=
ENST00000698863.1:c.1807C=	ENSP00000513991.1:p.Arg603=
ENST00000698864.1:n.2368C=
ENST00000698865.1:c.1828C=	ENSP00000513992.1:p.Arg610=
ENST00000698866.1:c.*1595C=	ENSP00000513993.1:n.*1595C=
ENST00000698867.1:n.5782C=
ENST00000698868.1:c.1672C=	ENSP00000513994.1:p.Arg558=
ENST00000698869.1:c.1573C=	ENSP00000513995.1:p.Arg525=
ENST00000698870.1:c.1807C=	ENSP00000513996.1:p.Arg603=
ENST00000698871.1:n.2330C=
ENST00000698872.1:c.*596C=	ENSP00000513997.1:n.*596C=
ENST00000698873.1:c.*1002C=	ENSP00000513998.1:n.*1002C=
ENST00000698874.1:c.1267C=	ENSP00000513999.1:p.Arg423=
ENST00000698875.1:n.1667C=
ENST00000698876.1:n.1855C=
ENST00000698877.1:n.1375C=
ENST00000698878.1:c.1801C=	ENSP00000514000.1:p.Arg601=
ENST00000698880.1:c.1675C=
ENST00000345728.10:c.1807C= MANE Select	ENSP00000339950.5:p.Arg603=
ENST00000279227.9:c.1819C=	ENSP00000279227.5:p.Arg607=
ENST00000345728.9:c.1807C=	ENSP00000339950.5:p.Arg603=
ENST00000545896.1:c.370C=	ENSP00000440209.1:p.Arg124=
NM_031471.5:c.1807C=	NP_113659.3:p.Arg603=
NM_178443.2:c.1819C= , LRG_180t1:c.1819C=	NP_848537.1:p.Arg607=
XM_011545294.1:c.1819C=	XP_011543596.1:p.Arg607=
XM_011545295.1:c.1279C=	XP_011543597.1:p.Arg427=
XM_011545296.1:c.1279C=	XP_011543598.1:p.Arg427=
XM_011545294.3:c.1819C=	XP_011543596.1:p.Arg607=
XM_011545295.2:c.1279C=	XP_011543597.1:p.Arg427=
XM_017018398.2:c.1807C=	XP_016873887.1:p.Arg603=
XM_017018399.1:c.1267C=	XP_016873888.1:p.Arg423=
NM_031471.6:c.1807C= MANE Select	NP_113659.3:p.Arg603=
NM_001382361.1:c.1807C=	NP_001369290.1:p.Arg603=
NM_001382362.1:c.1819C=	NP_001369291.1:p.Arg607=
NM_001382363.1:c.1267C=	NP_001369292.1:p.Arg423=
NM_001382364.1:c.1279C=	NP_001369293.1:p.Arg427=
NM_001382448.1:c.1807C=	NP_001369377.1:p.Arg603=
NM_178443.3:c.1819C=	NP_848537.1:p.Arg607=