Canonical Allele Identifier: CA1978638395
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220189_64220192delinsACCT , CM000673.2:g.64220189_64220192delinsACCT GRCh38
NC_000011.9:g.63987661_63987664delinsACCT , CM000673.1:g.63987661_63987664delinsACCT GRCh37
NC_000011.8:g.63744237_63744240delinsACCT NCBI36
NG_016360.1:g.18510_18513delinsACCT , LRG_180:g.18510_18513delinsACCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1217-31_1217-28delinsACCT ENSP00000279227.5:n.1217-31_1217-28delinsACCT
ENST00000540554.2:n.2274-31_2274-28delinsACCT
ENST00000541252.2:c.665-31_665-28delinsACCT ENSP00000438885.2:n.665-31_665-28delinsACCT
ENST00000541326.6:n.517-31_517-28delinsACCT
ENST00000544997.6:c.1205-31_1205-28delinsACCT ENSP00000445778.2:n.1205-31_1205-28delinsACCT
ENST00000546255.2:n.1400-31_1400-28delinsACCT
ENST00000698845.1:c.*400-31_*400-28delinsACCT ENSP00000513981.1:n.*400-31_*400-28delinsACCT
ENST00000698846.1:n.1342-31_1342-28delinsACCT
ENST00000698847.1:c.*610-31_*610-28delinsACCT ENSP00000513982.1:n.*610-31_*610-28delinsACCT
ENST00000698848.1:n.394-31_394-28delinsACCT
ENST00000698849.1:n.325-31_325-28delinsACCT
ENST00000698850.1:n.864-31_864-28delinsACCT
ENST00000698852.1:c.1205-31_1205-28delinsACCT ENSP00000513984.1:n.1205-31_1205-28delinsACCT
ENST00000698853.1:c.*434-31_*434-28delinsACCT ENSP00000513985.1:n.*434-31_*434-28delinsACCT
ENST00000698854.1:c.*535-31_*535-28delinsACCT ENSP00000513986.1:n.*535-31_*535-28delinsACCT
ENST00000698855.1:n.2857-31_2857-28delinsACCT
ENST00000698856.1:n.2442-31_2442-28delinsACCT
ENST00000698859.1:n.1369-31_1369-28delinsACCT
ENST00000698860.1:c.1217-31_1217-28delinsACCT ENSP00000513988.1:n.1217-31_1217-28delinsACCT
ENST00000698861.1:c.1205-31_1205-28delinsACCT ENSP00000513989.1:n.1205-31_1205-28delinsACCT
ENST00000698862.1:c.*501-31_*501-28delinsACCT ENSP00000513990.1:n.*501-31_*501-28delinsACCT
ENST00000698863.1:c.1205-31_1205-28delinsACCT ENSP00000513991.1:n.1205-31_1205-28delinsACCT
ENST00000698864.1:n.1311-31_1311-28delinsACCT
ENST00000698865.1:c.1226-31_1226-28delinsACCT ENSP00000513992.1:n.1226-31_1226-28delinsACCT
ENST00000698866.1:c.*610-31_*610-28delinsACCT ENSP00000513993.1:n.*610-31_*610-28delinsACCT
ENST00000698867.1:n.5180-31_5180-28delinsACCT
ENST00000698868.1:c.1070-31_1070-28delinsACCT ENSP00000513994.1:n.1070-31_1070-28delinsACCT
ENST00000698869.1:c.1205-31_1205-28delinsACCT ENSP00000513995.1:n.1205-31_1205-28delinsACCT
ENST00000698870.1:c.1205-31_1205-28delinsACCT ENSP00000513996.1:n.1205-31_1205-28delinsACCT
ENST00000698871.1:n.1728-31_1728-28delinsACCT
ENST00000698872.1:c.660-31_660-28delinsACCT ENSP00000513997.1:n.660-31_660-28delinsACCT
ENST00000698873.1:c.*400-31_*400-28delinsACCT ENSP00000513998.1:n.*400-31_*400-28delinsACCT
ENST00000698874.1:c.665-31_665-28delinsACCT ENSP00000513999.1:n.665-31_665-28delinsACCT
ENST00000698875.1:n.1065-31_1065-28delinsACCT
ENST00000698876.1:n.1144-31_1144-28delinsACCT
ENST00000698877.1:n.773-31_773-28delinsACCT
ENST00000698878.1:c.1205-31_1205-28delinsACCT ENSP00000514000.1:n.1205-31_1205-28delinsACCT
ENST00000698880.1:c.1045-31_1045-28delinsACCT
ENST00000345728.10:c.1205-31_1205-28delinsACCT MANE Select ENSP00000339950.5:n.1205-31_1205-28delinsACCT
ENST00000279227.9:c.1217-31_1217-28delinsACCT ENSP00000279227.5:n.1217-31_1217-28delinsACCT
ENST00000345728.9:c.1205-31_1205-28delinsACCT ENSP00000339950.5:n.1205-31_1205-28delinsACCT
ENST00000540957.1:n.358-31_358-28delinsACCT
ENST00000541326.5:n.512-31_512-28delinsACCT
NM_031471.5:c.1205-31_1205-28delinsACCT NP_113659.3:n.1205-31_1205-28delinsACCT
NM_178443.2:c.1217-31_1217-28delinsACCT , LRG_180t1:c.1217-31_1217-28delinsACCT NP_848537.1:n.1217-31_1217-28delinsACCT
XM_011545294.1:c.1217-31_1217-28delinsACCT XP_011543596.1:n.1217-31_1217-28delinsACCT
XM_011545295.1:c.677-31_677-28delinsACCT XP_011543597.1:n.677-31_677-28delinsACCT
XM_011545296.1:c.677-31_677-28delinsACCT XP_011543598.1:n.677-31_677-28delinsACCT
XM_011545294.3:c.1217-31_1217-28delinsACCT XP_011543596.1:n.1217-31_1217-28delinsACCT
XM_011545295.2:c.677-31_677-28delinsACCT XP_011543597.1:n.677-31_677-28delinsACCT
XM_017018398.2:c.1205-31_1205-28delinsACCT XP_016873887.1:n.1205-31_1205-28delinsACCT
XM_017018399.1:c.665-31_665-28delinsACCT XP_016873888.1:n.665-31_665-28delinsACCT
NM_031471.6:c.1205-31_1205-28delinsACCT MANE Select NP_113659.3:n.1205-31_1205-28delinsACCT
NM_001382361.1:c.1205-31_1205-28delinsACCT NP_001369290.1:n.1205-31_1205-28delinsACCT
NM_001382362.1:c.1217-31_1217-28delinsACCT NP_001369291.1:n.1217-31_1217-28delinsACCT
NM_001382363.1:c.665-31_665-28delinsACCT NP_001369292.1:n.665-31_665-28delinsACCT
NM_001382364.1:c.677-31_677-28delinsACCT NP_001369293.1:n.677-31_677-28delinsACCT
NM_001382448.1:c.1205-31_1205-28delinsACCT NP_001369377.1:n.1205-31_1205-28delinsACCT
NM_178443.3:c.1217-31_1217-28delinsACCT NP_848537.1:n.1217-31_1217-28delinsACCT