Canonical Allele Identifier: CA1978638576

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220285T= , CM000673.2:g.64220285T=	GRCh38
NC_000011.9:g.63987757T= , CM000673.1:g.63987757T=	GRCh37
NC_000011.8:g.63744333T=	NCBI36
NG_016360.1:g.18606T= , LRG_180:g.18606T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1282T=	ENSP00000279227.5:p.Ser428=
ENST00000540554.2:n.2339T=
ENST00000541252.2:c.730T=	ENSP00000438885.2:p.Ser244=
ENST00000541326.6:n.582T=
ENST00000544997.6:c.1270T=	ENSP00000445778.2:p.Ser424=
ENST00000546255.2:n.1465T=
ENST00000698845.1:c.*465T=	ENSP00000513981.1:n.*465T=
ENST00000698846.1:n.1407T=
ENST00000698847.1:c.*675T=	ENSP00000513982.1:n.*675T=
ENST00000698848.1:n.459T=
ENST00000698849.1:n.390T=
ENST00000698850.1:n.929T=
ENST00000698852.1:c.1270T=	ENSP00000513984.1:p.Ser424=
ENST00000698853.1:c.*499T=	ENSP00000513985.1:n.*499T=
ENST00000698854.1:c.*600T=	ENSP00000513986.1:n.*600T=
ENST00000698855.1:n.2922T=
ENST00000698856.1:n.2507T=
ENST00000698859.1:n.1434T=
ENST00000698860.1:c.1282T=	ENSP00000513988.1:p.Ser428=
ENST00000698861.1:c.1270T=	ENSP00000513989.1:p.Ser424=
ENST00000698862.1:c.*566T=	ENSP00000513990.1:n.*566T=
ENST00000698863.1:c.1270T=	ENSP00000513991.1:p.Ser424=
ENST00000698864.1:n.1376T=
ENST00000698865.1:c.1291T=	ENSP00000513992.1:p.Ser431=
ENST00000698866.1:c.*675T=	ENSP00000513993.1:n.*675T=
ENST00000698867.1:n.5245T=
ENST00000698868.1:c.1135T=	ENSP00000513994.1:p.Ser379=
ENST00000698869.1:c.1270T=	ENSP00000513995.1:p.Ser424=
ENST00000698870.1:c.1270T=	ENSP00000513996.1:p.Ser424=
ENST00000698871.1:n.1793T=
ENST00000698872.1:c.*59T=	ENSP00000513997.1:n.*59T=
ENST00000698873.1:c.*465T=	ENSP00000513998.1:n.*465T=
ENST00000698874.1:c.730T=	ENSP00000513999.1:p.Ser244=
ENST00000698875.1:n.1130T=
ENST00000698876.1:n.1209T=
ENST00000698877.1:n.838T=
ENST00000698878.1:c.1270T=	ENSP00000514000.1:p.Ser424=
ENST00000698880.1:c.1110T=
ENST00000345728.10:c.1270T= MANE Select	ENSP00000339950.5:p.Ser424=
ENST00000279227.9:c.1282T=	ENSP00000279227.5:p.Ser428=
ENST00000345728.9:c.1270T=	ENSP00000339950.5:p.Ser424=
ENST00000540957.1:n.423T=
ENST00000541326.5:n.577T=
NM_031471.5:c.1270T=	NP_113659.3:p.Ser424=
NM_178443.2:c.1282T= , LRG_180t1:c.1282T=	NP_848537.1:p.Ser428=
XM_011545294.1:c.1282T=	XP_011543596.1:p.Ser428=
XM_011545295.1:c.742T=	XP_011543597.1:p.Ser248=
XM_011545296.1:c.742T=	XP_011543598.1:p.Ser248=
XM_011545294.3:c.1282T=	XP_011543596.1:p.Ser428=
XM_011545295.2:c.742T=	XP_011543597.1:p.Ser248=
XM_017018398.2:c.1270T=	XP_016873887.1:p.Ser424=
XM_017018399.1:c.730T=	XP_016873888.1:p.Ser244=
NM_031471.6:c.1270T= MANE Select	NP_113659.3:p.Ser424=
NM_001382361.1:c.1270T=	NP_001369290.1:p.Ser424=
NM_001382362.1:c.1282T=	NP_001369291.1:p.Ser428=
NM_001382363.1:c.730T=	NP_001369292.1:p.Ser244=
NM_001382364.1:c.742T=	NP_001369293.1:p.Ser248=
NM_001382448.1:c.1270T=	NP_001369377.1:p.Ser424=
NM_178443.3:c.1282T=	NP_848537.1:p.Ser428=