Canonical Allele Identifier: CA2614110945
Gene: FERMT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220347_64220363dup , CM000673.2:g.64220347_64220363dup GRCh38
NC_000011.9:g.63987819_63987835dup , CM000673.1:g.63987819_63987835dup GRCh37
NC_000011.8:g.63744395_63744411dup NCBI36
NG_016360.1:g.18668_18684dup , LRG_180:g.18668_18684dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1323+21_1323+37dup ENSP00000279227.5:n.1323+21_1323+37dup
ENST00000540554.2:n.2401_2417dup
ENST00000541252.2:c.771+21_771+37dup ENSP00000438885.2:n.771+21_771+37dup
ENST00000541326.6:n.644_660dup
ENST00000544997.6:c.1311+21_1311+37dup ENSP00000445778.2:n.1311+21_1311+37dup
ENST00000546255.2:n.1527_1543dup
ENST00000698845.1:c.*506+21_*506+37dup ENSP00000513981.1:n.*506+21_*506+37dup
ENST00000698846.1:n.1469_1485dup
ENST00000698847.1:c.*716+21_*716+37dup ENSP00000513982.1:n.*716+21_*716+37dup
ENST00000698848.1:n.521_537dup
ENST00000698849.1:n.431+21_431+37dup
ENST00000698850.1:n.991_1007dup
ENST00000698852.1:c.1311+21_1311+37dup ENSP00000513984.1:n.1311+21_1311+37dup
ENST00000698853.1:c.*540+21_*540+37dup ENSP00000513985.1:n.*540+21_*540+37dup
ENST00000698854.1:c.*641+21_*641+37dup ENSP00000513986.1:n.*641+21_*641+37dup
ENST00000698855.1:n.2963+21_2963+37dup
ENST00000698856.1:n.2569_2585dup
ENST00000698859.1:n.1475+21_1475+37dup
ENST00000698860.1:c.1323+21_1323+37dup ENSP00000513988.1:n.1323+21_1323+37dup
ENST00000698861.1:c.1311+21_1311+37dup ENSP00000513989.1:n.1311+21_1311+37dup
ENST00000698862.1:c.*607+21_*607+37dup ENSP00000513990.1:n.*607+21_*607+37dup
ENST00000698863.1:c.1311+21_1311+37dup ENSP00000513991.1:n.1311+21_1311+37dup
ENST00000698864.1:n.1438_1454dup
ENST00000698865.1:c.1332+21_1332+37dup ENSP00000513992.1:n.1332+21_1332+37dup
ENST00000698866.1:c.*737_*753dup ENSP00000513993.1:n.*737_*753dup
ENST00000698867.1:n.5286+21_5286+37dup
ENST00000698868.1:c.1176+21_1176+37dup ENSP00000513994.1:n.1176+21_1176+37dup
ENST00000698869.1:c.1311+21_1311+37dup ENSP00000513995.1:n.1311+21_1311+37dup
ENST00000698870.1:c.1311+21_1311+37dup ENSP00000513996.1:n.1311+21_1311+37dup
ENST00000698871.1:n.1834+21_1834+37dup
ENST00000698872.1:c.*100+21_*100+37dup ENSP00000513997.1:n.*100+21_*100+37dup
ENST00000698873.1:c.*506+21_*506+37dup ENSP00000513998.1:n.*506+21_*506+37dup
ENST00000698874.1:c.771+21_771+37dup ENSP00000513999.1:n.771+21_771+37dup
ENST00000698875.1:n.1171+21_1171+37dup
ENST00000698876.1:n.1271_1287dup
ENST00000698877.1:n.879+21_879+37dup
ENST00000698878.1:c.1311+21_1311+37dup ENSP00000514000.1:n.1311+21_1311+37dup
ENST00000698880.1:c.1151+21_1151+37dup
ENST00000345728.10:c.1311+21_1311+37dup MANE Select ENSP00000339950.5:n.1311+21_1311+37dup
ENST00000279227.9:c.1323+21_1323+37dup ENSP00000279227.5:n.1323+21_1323+37dup
ENST00000345728.9:c.1311+21_1311+37dup ENSP00000339950.5:n.1311+21_1311+37dup
ENST00000540957.1:n.485_501dup
ENST00000541326.5:n.639_655dup
NM_031471.5:c.1311+21_1311+37dup NP_113659.3:n.1311+21_1311+37dup
NM_178443.2:c.1323+21_1323+37dup , LRG_180t1:c.1323+21_1323+37dup NP_848537.1:n.1323+21_1323+37dup
XM_011545294.1:c.1323+21_1323+37dup XP_011543596.1:n.1323+21_1323+37dup
XM_011545295.1:c.783+21_783+37dup XP_011543597.1:n.783+21_783+37dup
XM_011545296.1:c.783+21_783+37dup XP_011543598.1:n.783+21_783+37dup
XM_011545294.3:c.1323+21_1323+37dup XP_011543596.1:n.1323+21_1323+37dup
XM_011545295.2:c.783+21_783+37dup XP_011543597.1:n.783+21_783+37dup
XM_017018398.2:c.1311+21_1311+37dup XP_016873887.1:n.1311+21_1311+37dup
XM_017018399.1:c.771+21_771+37dup XP_016873888.1:n.771+21_771+37dup
NM_031471.6:c.1311+21_1311+37dup MANE Select NP_113659.3:n.1311+21_1311+37dup
NM_001382361.1:c.1311+21_1311+37dup NP_001369290.1:n.1311+21_1311+37dup
NM_001382362.1:c.1323+21_1323+37dup NP_001369291.1:n.1323+21_1323+37dup
NM_001382363.1:c.771+21_771+37dup NP_001369292.1:n.771+21_771+37dup
NM_001382364.1:c.783+21_783+37dup NP_001369293.1:n.783+21_783+37dup
NM_001382448.1:c.1311+21_1311+37dup NP_001369377.1:n.1311+21_1311+37dup
NM_178443.3:c.1323+21_1323+37dup NP_848537.1:n.1323+21_1323+37dup