Canonical Allele Identifier: CA1978643001

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223183C= , CM000673.2:g.64223183C=	GRCh38
NC_000011.9:g.63990655C= , CM000673.1:g.63990655C=	GRCh37
NC_000011.8:g.63747231C=	NCBI36
NG_016360.1:g.21504C= , LRG_180:g.21504C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1818C=	ENSP00000279227.5:p.Ile606=
ENST00000540554.2:n.3330C=
ENST00000541252.2:c.1266C=	ENSP00000438885.2:p.Ile422=
ENST00000544997.6:c.1806C=	ENSP00000445778.2:p.Ile602=
ENST00000545896.2:c.370C=	ENSP00000440209.2:p.Pro124=
ENST00000546255.2:n.2110C=
ENST00000698845.1:c.*1001C=	ENSP00000513981.1:n.*1001C=
ENST00000698846.1:n.2052C=
ENST00000698847.1:c.*1211C=	ENSP00000513982.1:n.*1211C=
ENST00000698850.1:n.3827C=
ENST00000698852.1:c.1806C=	ENSP00000513984.1:p.Ile602=
ENST00000698853.1:c.*1035C=	ENSP00000513985.1:n.*1035C=
ENST00000698854.1:c.*1136C=	ENSP00000513986.1:n.*1136C=
ENST00000698855.1:n.3458C=
ENST00000698856.1:n.3152C=
ENST00000698859.1:n.2316C=
ENST00000698860.1:c.1818C=	ENSP00000513988.1:p.Ile606=
ENST00000698861.1:c.1806C=	ENSP00000513989.1:p.Ile602=
ENST00000698862.1:c.*1102C=	ENSP00000513990.1:n.*1102C=
ENST00000698863.1:c.1806C=	ENSP00000513991.1:p.Ile602=
ENST00000698864.1:n.2367C=
ENST00000698865.1:c.1827C=	ENSP00000513992.1:p.Ile609=
ENST00000698866.1:c.*1594C=	ENSP00000513993.1:n.*1594C=
ENST00000698867.1:n.5781C=
ENST00000698868.1:c.1671C=	ENSP00000513994.1:p.Ile557=
ENST00000698869.1:c.1572C=	ENSP00000513995.1:p.Ile524=
ENST00000698870.1:c.1806C=	ENSP00000513996.1:p.Ile602=
ENST00000698871.1:n.2329C=
ENST00000698872.1:c.*595C=	ENSP00000513997.1:n.*595C=
ENST00000698873.1:c.*1001C=	ENSP00000513998.1:n.*1001C=
ENST00000698874.1:c.1266C=	ENSP00000513999.1:p.Ile422=
ENST00000698875.1:n.1666C=
ENST00000698876.1:n.1854C=
ENST00000698877.1:n.1374C=
ENST00000698878.1:c.1800C=	ENSP00000514000.1:p.Ile600=
ENST00000698880.1:c.1674C=
ENST00000345728.10:c.1806C= MANE Select	ENSP00000339950.5:p.Ile602=
ENST00000279227.9:c.1818C=	ENSP00000279227.5:p.Ile606=
ENST00000345728.9:c.1806C=	ENSP00000339950.5:p.Ile602=
ENST00000545896.1:c.369C=	ENSP00000440209.1:p.Ile123=
NM_031471.5:c.1806C=	NP_113659.3:p.Ile602=
NM_178443.2:c.1818C= , LRG_180t1:c.1818C=	NP_848537.1:p.Ile606=
XM_011545294.1:c.1818C=	XP_011543596.1:p.Ile606=
XM_011545295.1:c.1278C=	XP_011543597.1:p.Ile426=
XM_011545296.1:c.1278C=	XP_011543598.1:p.Ile426=
XM_011545294.3:c.1818C=	XP_011543596.1:p.Ile606=
XM_011545295.2:c.1278C=	XP_011543597.1:p.Ile426=
XM_017018398.2:c.1806C=	XP_016873887.1:p.Ile602=
XM_017018399.1:c.1266C=	XP_016873888.1:p.Ile422=
NM_031471.6:c.1806C= MANE Select	NP_113659.3:p.Ile602=
NM_001382361.1:c.1806C=	NP_001369290.1:p.Ile602=
NM_001382362.1:c.1818C=	NP_001369291.1:p.Ile606=
NM_001382363.1:c.1266C=	NP_001369292.1:p.Ile422=
NM_001382364.1:c.1278C=	NP_001369293.1:p.Ile426=
NM_001382448.1:c.1806C=	NP_001369377.1:p.Ile602=
NM_178443.3:c.1818C=	NP_848537.1:p.Ile606=