Canonical Allele Identifier: CA2574859369

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220342del , CM000673.2:g.64220342del	GRCh38
NC_000011.9:g.63987814del , CM000673.1:g.63987814del	GRCh37
NC_000011.8:g.63744390del	NCBI36
NG_016360.1:g.18663del , LRG_180:g.18663del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1323+16del	ENSP00000279227.5:n.1323+16del
ENST00000540554.2:n.2396del
ENST00000541252.2:c.771+16del	ENSP00000438885.2:n.771+16del
ENST00000541326.6:n.639del
ENST00000544997.6:c.1311+16del	ENSP00000445778.2:n.1311+16del
ENST00000546255.2:n.1522del
ENST00000698845.1:c.*506+16del	ENSP00000513981.1:n.*506+16del
ENST00000698846.1:n.1464del
ENST00000698847.1:c.*716+16del	ENSP00000513982.1:n.*716+16del
ENST00000698848.1:n.516del
ENST00000698849.1:n.431+16del
ENST00000698850.1:n.986del
ENST00000698852.1:c.1311+16del	ENSP00000513984.1:n.1311+16del
ENST00000698853.1:c.*540+16del	ENSP00000513985.1:n.*540+16del
ENST00000698854.1:c.*641+16del	ENSP00000513986.1:n.*641+16del
ENST00000698855.1:n.2963+16del
ENST00000698856.1:n.2564del
ENST00000698859.1:n.1475+16del
ENST00000698860.1:c.1323+16del	ENSP00000513988.1:n.1323+16del
ENST00000698861.1:c.1311+16del	ENSP00000513989.1:n.1311+16del
ENST00000698862.1:c.*607+16del	ENSP00000513990.1:n.*607+16del
ENST00000698863.1:c.1311+16del	ENSP00000513991.1:n.1311+16del
ENST00000698864.1:n.1433del
ENST00000698865.1:c.1332+16del	ENSP00000513992.1:n.1332+16del
ENST00000698866.1:c.*732del	ENSP00000513993.1:n.*732del
ENST00000698867.1:n.5286+16del
ENST00000698868.1:c.1176+16del	ENSP00000513994.1:n.1176+16del
ENST00000698869.1:c.1311+16del	ENSP00000513995.1:n.1311+16del
ENST00000698870.1:c.1311+16del	ENSP00000513996.1:n.1311+16del
ENST00000698871.1:n.1834+16del
ENST00000698872.1:c.*100+16del	ENSP00000513997.1:n.*100+16del
ENST00000698873.1:c.*506+16del	ENSP00000513998.1:n.*506+16del
ENST00000698874.1:c.771+16del	ENSP00000513999.1:n.771+16del
ENST00000698875.1:n.1171+16del
ENST00000698876.1:n.1266del
ENST00000698877.1:n.879+16del
ENST00000698878.1:c.1311+16del	ENSP00000514000.1:n.1311+16del
ENST00000698880.1:c.1151+16del
ENST00000345728.10:c.1311+16del MANE Select	ENSP00000339950.5:n.1311+16del
ENST00000279227.9:c.1323+16del	ENSP00000279227.5:n.1323+16del
ENST00000345728.9:c.1311+16del	ENSP00000339950.5:n.1311+16del
ENST00000540957.1:n.480del
ENST00000541326.5:n.634del
NM_031471.5:c.1311+16del	NP_113659.3:n.1311+16del
NM_178443.2:c.1323+16del , LRG_180t1:c.1323+16del	NP_848537.1:n.1323+16del
XM_011545294.1:c.1323+16del	XP_011543596.1:n.1323+16del
XM_011545295.1:c.783+16del	XP_011543597.1:n.783+16del
XM_011545296.1:c.783+16del	XP_011543598.1:n.783+16del
XM_011545294.3:c.1323+16del	XP_011543596.1:n.1323+16del
XM_011545295.2:c.783+16del	XP_011543597.1:n.783+16del
XM_017018398.2:c.1311+16del	XP_016873887.1:n.1311+16del
XM_017018399.1:c.771+16del	XP_016873888.1:n.771+16del
NM_031471.6:c.1311+16del MANE Select	NP_113659.3:n.1311+16del
NM_001382361.1:c.1311+16del	NP_001369290.1:n.1311+16del
NM_001382362.1:c.1323+16del	NP_001369291.1:n.1323+16del
NM_001382363.1:c.771+16del	NP_001369292.1:n.771+16del
NM_001382364.1:c.783+16del	NP_001369293.1:n.783+16del
NM_001382448.1:c.1311+16del	NP_001369377.1:n.1311+16del
NM_178443.3:c.1323+16del	NP_848537.1:n.1323+16del