Canonical Allele Identifier: CA599800784

Gene: FERMT3

Linked Data

• dbSNP Id: rs1591039784
• gnomAD v2: 11-63987798-TGTGA-T
• gnomAD v4: 11-64220326-TGTGA-T
• MyVariant Identifiers: chr11:g.63987799_63987802del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220332_64220335del , CM000673.2:g.64220332_64220335del	GRCh38
NC_000011.9:g.63987804_63987807del , CM000673.1:g.63987804_63987807del	GRCh37
NC_000011.8:g.63744380_63744383del	NCBI36
NG_016360.1:g.18653_18656del , LRG_180:g.18653_18656del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1323+6_1323+9del	ENSP00000279227.5:n.1323+6_1323+9del
ENST00000540554.2:n.2386_2389del
ENST00000541252.2:c.771+6_771+9del	ENSP00000438885.2:n.771+6_771+9del
ENST00000541326.6:n.629_632del
ENST00000544997.6:c.1311+6_1311+9del	ENSP00000445778.2:n.1311+6_1311+9del
ENST00000546255.2:n.1512_1515del
ENST00000698845.1:c.*506+6_*506+9del	ENSP00000513981.1:n.*506+6_*506+9del
ENST00000698846.1:n.1454_1457del
ENST00000698847.1:c.*716+6_*716+9del	ENSP00000513982.1:n.*716+6_*716+9del
ENST00000698848.1:n.506_509del
ENST00000698849.1:n.431+6_431+9del
ENST00000698850.1:n.976_979del
ENST00000698852.1:c.1311+6_1311+9del	ENSP00000513984.1:n.1311+6_1311+9del
ENST00000698853.1:c.*540+6_*540+9del	ENSP00000513985.1:n.*540+6_*540+9del
ENST00000698854.1:c.*641+6_*641+9del	ENSP00000513986.1:n.*641+6_*641+9del
ENST00000698855.1:n.2963+6_2963+9del
ENST00000698856.1:n.2554_2557del
ENST00000698859.1:n.1475+6_1475+9del
ENST00000698860.1:c.1323+6_1323+9del	ENSP00000513988.1:n.1323+6_1323+9del
ENST00000698861.1:c.1311+6_1311+9del	ENSP00000513989.1:n.1311+6_1311+9del
ENST00000698862.1:c.*607+6_*607+9del	ENSP00000513990.1:n.*607+6_*607+9del
ENST00000698863.1:c.1311+6_1311+9del	ENSP00000513991.1:n.1311+6_1311+9del
ENST00000698864.1:n.1423_1426del
ENST00000698865.1:c.1332+6_1332+9del	ENSP00000513992.1:n.1332+6_1332+9del
ENST00000698866.1:c.*722_*725del	ENSP00000513993.1:n.*722_*725del
ENST00000698867.1:n.5286+6_5286+9del
ENST00000698868.1:c.1176+6_1176+9del	ENSP00000513994.1:n.1176+6_1176+9del
ENST00000698869.1:c.1311+6_1311+9del	ENSP00000513995.1:n.1311+6_1311+9del
ENST00000698870.1:c.1311+6_1311+9del	ENSP00000513996.1:n.1311+6_1311+9del
ENST00000698871.1:n.1834+6_1834+9del
ENST00000698872.1:c.*100+6_*100+9del	ENSP00000513997.1:n.*100+6_*100+9del
ENST00000698873.1:c.*506+6_*506+9del	ENSP00000513998.1:n.*506+6_*506+9del
ENST00000698874.1:c.771+6_771+9del	ENSP00000513999.1:n.771+6_771+9del
ENST00000698875.1:n.1171+6_1171+9del
ENST00000698876.1:n.1256_1259del
ENST00000698877.1:n.879+6_879+9del
ENST00000698878.1:c.1311+6_1311+9del	ENSP00000514000.1:n.1311+6_1311+9del
ENST00000698880.1:c.1151+6_1151+9del
ENST00000345728.10:c.1311+6_1311+9del MANE Select	ENSP00000339950.5:n.1311+6_1311+9del
ENST00000279227.9:c.1323+6_1323+9del	ENSP00000279227.5:n.1323+6_1323+9del
ENST00000345728.9:c.1311+6_1311+9del	ENSP00000339950.5:n.1311+6_1311+9del
ENST00000540957.1:n.470_473del
ENST00000541326.5:n.624_627del
NM_031471.5:c.1311+6_1311+9del	NP_113659.3:n.1311+6_1311+9del
NM_178443.2:c.1323+6_1323+9del , LRG_180t1:c.1323+6_1323+9del	NP_848537.1:n.1323+6_1323+9del
XM_011545294.1:c.1323+6_1323+9del	XP_011543596.1:n.1323+6_1323+9del
XM_011545295.1:c.783+6_783+9del	XP_011543597.1:n.783+6_783+9del
XM_011545296.1:c.783+6_783+9del	XP_011543598.1:n.783+6_783+9del
XM_011545294.3:c.1323+6_1323+9del	XP_011543596.1:n.1323+6_1323+9del
XM_011545295.2:c.783+6_783+9del	XP_011543597.1:n.783+6_783+9del
XM_017018398.2:c.1311+6_1311+9del	XP_016873887.1:n.1311+6_1311+9del
XM_017018399.1:c.771+6_771+9del	XP_016873888.1:n.771+6_771+9del
NM_031471.6:c.1311+6_1311+9del MANE Select	NP_113659.3:n.1311+6_1311+9del
NM_001382361.1:c.1311+6_1311+9del	NP_001369290.1:n.1311+6_1311+9del
NM_001382362.1:c.1323+6_1323+9del	NP_001369291.1:n.1323+6_1323+9del
NM_001382363.1:c.771+6_771+9del	NP_001369292.1:n.771+6_771+9del
NM_001382364.1:c.783+6_783+9del	NP_001369293.1:n.783+6_783+9del
NM_001382448.1:c.1311+6_1311+9del	NP_001369377.1:n.1311+6_1311+9del
NM_178443.3:c.1323+6_1323+9del	NP_848537.1:n.1323+6_1323+9del