Canonical Allele Identifier: CA1978638460

Gene: FERMT3

Linked Data

• dbSNP Id: rs1946648461

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220215dup , CM000673.2:g.64220215dup	GRCh38
NC_000011.9:g.63987687dup , CM000673.1:g.63987687dup	GRCh37
NC_000011.8:g.63744263dup	NCBI36
NG_016360.1:g.18536dup , LRG_180:g.18536dup

Transcript Alleles

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