Canonical Allele Identifier: CA1978638955

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220506G= , CM000673.2:g.64220506G=	GRCh38
NC_000011.9:g.63987978G= , CM000673.1:g.63987978G=	GRCh37
NC_000011.8:g.63744554G=	NCBI36
NG_016360.1:g.18827G= , LRG_180:g.18827G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1394G=	ENSP00000279227.5:p.Ser465=
ENST00000540554.2:n.2560G=
ENST00000541252.2:c.842G=	ENSP00000438885.2:p.Ser281=
ENST00000541326.6:n.803G=
ENST00000544997.6:c.1382G=	ENSP00000445778.2:p.Ser461=
ENST00000545896.2:c.71G=	ENSP00000440209.2:p.Ser24=
ENST00000546255.2:n.1686G=
ENST00000698845.1:c.*577G=	ENSP00000513981.1:n.*577G=
ENST00000698846.1:n.1628G=
ENST00000698847.1:c.*787G=	ENSP00000513982.1:n.*787G=
ENST00000698849.1:n.502G=
ENST00000698850.1:n.1150G=
ENST00000698852.1:c.1382G=	ENSP00000513984.1:p.Ser461=
ENST00000698853.1:c.*611G=	ENSP00000513985.1:n.*611G=
ENST00000698854.1:c.*712G=	ENSP00000513986.1:n.*712G=
ENST00000698855.1:n.3034G=
ENST00000698856.1:n.2728G=
ENST00000698859.1:n.1546G=
ENST00000698860.1:c.1394G=	ENSP00000513988.1:p.Ser465=
ENST00000698861.1:c.1382G=	ENSP00000513989.1:p.Ser461=
ENST00000698862.1:c.*678G=	ENSP00000513990.1:n.*678G=
ENST00000698863.1:c.1382G=	ENSP00000513991.1:p.Ser461=
ENST00000698864.1:n.1597G=
ENST00000698865.1:c.1403G=	ENSP00000513992.1:p.Ser468=
ENST00000698866.1:c.*896G=	ENSP00000513993.1:n.*896G=
ENST00000698867.1:n.5357G=
ENST00000698868.1:c.1247G=	ENSP00000513994.1:p.Ser416=
ENST00000698869.1:c.1311+180G=	ENSP00000513995.1:n.1311+180G=
ENST00000698870.1:c.1382G=	ENSP00000513996.1:p.Ser461=
ENST00000698871.1:n.1905G=
ENST00000698872.1:c.*171G=	ENSP00000513997.1:n.*171G=
ENST00000698873.1:c.*577G=	ENSP00000513998.1:n.*577G=
ENST00000698874.1:c.842G=	ENSP00000513999.1:p.Ser281=
ENST00000698875.1:n.1242G=
ENST00000698876.1:n.1430G=
ENST00000698877.1:n.950G=
ENST00000698878.1:c.1376G=	ENSP00000514000.1:p.Ser459=
ENST00000698880.1:c.1250G=
ENST00000345728.10:c.1382G= MANE Select	ENSP00000339950.5:p.Ser461=
ENST00000279227.9:c.1394G=	ENSP00000279227.5:p.Ser465=
ENST00000345728.9:c.1382G=	ENSP00000339950.5:p.Ser461=
ENST00000541326.5:n.798G=
ENST00000545896.1:c.70G=	ENSP00000440209.1:p.Ala24=
NM_031471.5:c.1382G=	NP_113659.3:p.Ser461=
NM_178443.2:c.1394G= , LRG_180t1:c.1394G=	NP_848537.1:p.Ser465=
XM_011545294.1:c.1394G=	XP_011543596.1:p.Ser465=
XM_011545295.1:c.854G=	XP_011543597.1:p.Ser285=
XM_011545296.1:c.854G=	XP_011543598.1:p.Ser285=
XM_011545294.3:c.1394G=	XP_011543596.1:p.Ser465=
XM_011545295.2:c.854G=	XP_011543597.1:p.Ser285=
XM_017018398.2:c.1382G=	XP_016873887.1:p.Ser461=
XM_017018399.1:c.842G=	XP_016873888.1:p.Ser281=
NM_031471.6:c.1382G= MANE Select	NP_113659.3:p.Ser461=
NM_001382361.1:c.1382G=	NP_001369290.1:p.Ser461=
NM_001382362.1:c.1394G=	NP_001369291.1:p.Ser465=
NM_001382363.1:c.842G=	NP_001369292.1:p.Ser281=
NM_001382364.1:c.854G=	NP_001369293.1:p.Ser285=
NM_001382448.1:c.1382G=	NP_001369377.1:p.Ser461=
NM_178443.3:c.1394G=	NP_848537.1:p.Ser465=