Canonical Allele Identifier: CA1978638580

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220289_64220290delinsCT , CM000673.2:g.64220289_64220290delinsCT	GRCh38
NC_000011.9:g.63987761_63987762delinsCT , CM000673.1:g.63987761_63987762delinsCT	GRCh37
NC_000011.8:g.63744337_63744338delinsCT	NCBI36
NG_016360.1:g.18610_18611delinsCT , LRG_180:g.18610_18611delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1286_1287delinsCT	ENSP00000279227.5:p.Pro429=
ENST00000540554.2:n.2343_2344delinsCT
ENST00000541252.2:c.734_735delinsCT	ENSP00000438885.2:p.Pro245=
ENST00000541326.6:n.586_587delinsCT
ENST00000544997.6:c.1274_1275delinsCT	ENSP00000445778.2:p.Pro425=
ENST00000546255.2:n.1469_1470delinsCT
ENST00000698845.1:c.*469_*470delinsCT	ENSP00000513981.1:n.*469_*470delinsCT
ENST00000698846.1:n.1411_1412delinsCT
ENST00000698847.1:c.*679_*680delinsCT	ENSP00000513982.1:n.*679_*680delinsCT
ENST00000698848.1:n.463_464delinsCT
ENST00000698849.1:n.394_395delinsCT
ENST00000698850.1:n.933_934delinsCT
ENST00000698852.1:c.1274_1275delinsCT	ENSP00000513984.1:p.Pro425=
ENST00000698853.1:c.*503_*504delinsCT	ENSP00000513985.1:n.*503_*504delinsCT
ENST00000698854.1:c.*604_*605delinsCT	ENSP00000513986.1:n.*604_*605delinsCT
ENST00000698855.1:n.2926_2927delinsCT
ENST00000698856.1:n.2511_2512delinsCT
ENST00000698859.1:n.1438_1439delinsCT
ENST00000698860.1:c.1286_1287delinsCT	ENSP00000513988.1:p.Pro429=
ENST00000698861.1:c.1274_1275delinsCT	ENSP00000513989.1:p.Pro425=
ENST00000698862.1:c.*570_*571delinsCT	ENSP00000513990.1:n.*570_*571delinsCT
ENST00000698863.1:c.1274_1275delinsCT	ENSP00000513991.1:p.Pro425=
ENST00000698864.1:n.1380_1381delinsCT
ENST00000698865.1:c.1295_1296delinsCT	ENSP00000513992.1:p.Pro432=
ENST00000698866.1:c.*679_*680delinsCT	ENSP00000513993.1:n.*679_*680delinsCT
ENST00000698867.1:n.5249_5250delinsCT
ENST00000698868.1:c.1139_1140delinsCT	ENSP00000513994.1:p.Pro380=
ENST00000698869.1:c.1274_1275delinsCT	ENSP00000513995.1:p.Pro425=
ENST00000698870.1:c.1274_1275delinsCT	ENSP00000513996.1:p.Pro425=
ENST00000698871.1:n.1797_1798delinsCT
ENST00000698872.1:c.*63_*64delinsCT	ENSP00000513997.1:n.*63_*64delinsCT
ENST00000698873.1:c.*469_*470delinsCT	ENSP00000513998.1:n.*469_*470delinsCT
ENST00000698874.1:c.734_735delinsCT	ENSP00000513999.1:p.Pro245=
ENST00000698875.1:n.1134_1135delinsCT
ENST00000698876.1:n.1213_1214delinsCT
ENST00000698877.1:n.842_843delinsCT
ENST00000698878.1:c.1274_1275delinsCT	ENSP00000514000.1:p.Pro425=
ENST00000698880.1:c.1114_1115delinsCT
ENST00000345728.10:c.1274_1275delinsCT MANE Select	ENSP00000339950.5:p.Pro425=
ENST00000279227.9:c.1286_1287delinsCT	ENSP00000279227.5:p.Pro429=
ENST00000345728.9:c.1274_1275delinsCT	ENSP00000339950.5:p.Pro425=
ENST00000540957.1:n.427_428delinsCT
ENST00000541326.5:n.581_582delinsCT
NM_031471.5:c.1274_1275delinsCT	NP_113659.3:p.Pro425=
NM_178443.2:c.1286_1287delinsCT , LRG_180t1:c.1286_1287delinsCT	NP_848537.1:p.Pro429=
XM_011545294.1:c.1286_1287delinsCT	XP_011543596.1:p.Pro429=
XM_011545295.1:c.746_747delinsCT	XP_011543597.1:p.Pro249=
XM_011545296.1:c.746_747delinsCT	XP_011543598.1:p.Pro249=
XM_011545294.3:c.1286_1287delinsCT	XP_011543596.1:p.Pro429=
XM_011545295.2:c.746_747delinsCT	XP_011543597.1:p.Pro249=
XM_017018398.2:c.1274_1275delinsCT	XP_016873887.1:p.Pro425=
XM_017018399.1:c.734_735delinsCT	XP_016873888.1:p.Pro245=
NM_031471.6:c.1274_1275delinsCT MANE Select	NP_113659.3:p.Pro425=
NM_001382361.1:c.1274_1275delinsCT	NP_001369290.1:p.Pro425=
NM_001382362.1:c.1286_1287delinsCT	NP_001369291.1:p.Pro429=
NM_001382363.1:c.734_735delinsCT	NP_001369292.1:p.Pro245=
NM_001382364.1:c.746_747delinsCT	NP_001369293.1:p.Pro249=
NM_001382448.1:c.1274_1275delinsCT	NP_001369377.1:p.Pro425=
NM_178443.3:c.1286_1287delinsCT	NP_848537.1:p.Pro429=