Canonical Allele Identifier: CA1978638674

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220344A= , CM000673.2:g.64220344A=	GRCh38
NC_000011.9:g.63987816A= , CM000673.1:g.63987816A=	GRCh37
NC_000011.8:g.63744392A=	NCBI36
NG_016360.1:g.18665A= , LRG_180:g.18665A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1323+18A=	ENSP00000279227.5:n.1323+18A=
ENST00000540554.2:n.2398A=
ENST00000541252.2:c.771+18A=	ENSP00000438885.2:n.771+18A=
ENST00000541326.6:n.641A=
ENST00000544997.6:c.1311+18A=	ENSP00000445778.2:n.1311+18A=
ENST00000546255.2:n.1524A=
ENST00000698845.1:c.*506+18A=	ENSP00000513981.1:n.*506+18A=
ENST00000698846.1:n.1466A=
ENST00000698847.1:c.*716+18A=	ENSP00000513982.1:n.*716+18A=
ENST00000698848.1:n.518A=
ENST00000698849.1:n.431+18A=
ENST00000698850.1:n.988A=
ENST00000698852.1:c.1311+18A=	ENSP00000513984.1:n.1311+18A=
ENST00000698853.1:c.*540+18A=	ENSP00000513985.1:n.*540+18A=
ENST00000698854.1:c.*641+18A=	ENSP00000513986.1:n.*641+18A=
ENST00000698855.1:n.2963+18A=
ENST00000698856.1:n.2566A=
ENST00000698859.1:n.1475+18A=
ENST00000698860.1:c.1323+18A=	ENSP00000513988.1:n.1323+18A=
ENST00000698861.1:c.1311+18A=	ENSP00000513989.1:n.1311+18A=
ENST00000698862.1:c.*607+18A=	ENSP00000513990.1:n.*607+18A=
ENST00000698863.1:c.1311+18A=	ENSP00000513991.1:n.1311+18A=
ENST00000698864.1:n.1435A=
ENST00000698865.1:c.1332+18A=	ENSP00000513992.1:n.1332+18A=
ENST00000698866.1:c.*734A=	ENSP00000513993.1:n.*734A=
ENST00000698867.1:n.5286+18A=
ENST00000698868.1:c.1176+18A=	ENSP00000513994.1:n.1176+18A=
ENST00000698869.1:c.1311+18A=	ENSP00000513995.1:n.1311+18A=
ENST00000698870.1:c.1311+18A=	ENSP00000513996.1:n.1311+18A=
ENST00000698871.1:n.1834+18A=
ENST00000698872.1:c.*100+18A=	ENSP00000513997.1:n.*100+18A=
ENST00000698873.1:c.*506+18A=	ENSP00000513998.1:n.*506+18A=
ENST00000698874.1:c.771+18A=	ENSP00000513999.1:n.771+18A=
ENST00000698875.1:n.1171+18A=
ENST00000698876.1:n.1268A=
ENST00000698877.1:n.879+18A=
ENST00000698878.1:c.1311+18A=	ENSP00000514000.1:n.1311+18A=
ENST00000698880.1:c.1151+18A=
ENST00000345728.10:c.1311+18A= MANE Select	ENSP00000339950.5:n.1311+18A=
ENST00000279227.9:c.1323+18A=	ENSP00000279227.5:n.1323+18A=
ENST00000345728.9:c.1311+18A=	ENSP00000339950.5:n.1311+18A=
ENST00000540957.1:n.482A=
ENST00000541326.5:n.636A=
NM_031471.5:c.1311+18A=	NP_113659.3:n.1311+18A=
NM_178443.2:c.1323+18A= , LRG_180t1:c.1323+18A=	NP_848537.1:n.1323+18A=
XM_011545294.1:c.1323+18A=	XP_011543596.1:n.1323+18A=
XM_011545295.1:c.783+18A=	XP_011543597.1:n.783+18A=
XM_011545296.1:c.783+18A=	XP_011543598.1:n.783+18A=
XM_011545294.3:c.1323+18A=	XP_011543596.1:n.1323+18A=
XM_011545295.2:c.783+18A=	XP_011543597.1:n.783+18A=
XM_017018398.2:c.1311+18A=	XP_016873887.1:n.1311+18A=
XM_017018399.1:c.771+18A=	XP_016873888.1:n.771+18A=
NM_031471.6:c.1311+18A= MANE Select	NP_113659.3:n.1311+18A=
NM_001382361.1:c.1311+18A=	NP_001369290.1:n.1311+18A=
NM_001382362.1:c.1323+18A=	NP_001369291.1:n.1323+18A=
NM_001382363.1:c.771+18A=	NP_001369292.1:n.771+18A=
NM_001382364.1:c.783+18A=	NP_001369293.1:n.783+18A=
NM_001382448.1:c.1311+18A=	NP_001369377.1:n.1311+18A=
NM_178443.3:c.1323+18A=	NP_848537.1:n.1323+18A=