Canonical Allele Identifier: CA381087968

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63988054C>G (hg19) ; chr11:g.64220582C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220582C>G , CM000673.2:g.64220582C>G	GRCh38
NC_000011.9:g.63988054C>G , CM000673.1:g.63988054C>G	GRCh37
NC_000011.8:g.63744630C>G	NCBI36
NG_016360.1:g.18903C>G , LRG_180:g.18903C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1470C>G	ENSP00000279227.5:p.His490Gln
ENST00000540554.2:n.2636C>G
ENST00000541252.2:c.918C>G	ENSP00000438885.2:p.His306Gln
ENST00000541326.6:n.879C>G
ENST00000544997.6:c.1458C>G	ENSP00000445778.2:p.His486Gln
ENST00000545896.2:c.147C>G	ENSP00000440209.2:p.His49Gln
ENST00000546255.2:n.1762C>G
ENST00000698845.1:c.*653C>G	ENSP00000513981.1:n.*653C>G
ENST00000698846.1:n.1704C>G
ENST00000698847.1:c.*863C>G	ENSP00000513982.1:n.*863C>G
ENST00000698849.1:n.578C>G
ENST00000698850.1:n.1226C>G
ENST00000698852.1:c.1458C>G	ENSP00000513984.1:p.His486Gln
ENST00000698853.1:c.*687C>G	ENSP00000513985.1:n.*687C>G
ENST00000698854.1:c.*788C>G	ENSP00000513986.1:n.*788C>G
ENST00000698855.1:n.3110C>G
ENST00000698856.1:n.2804C>G
ENST00000698859.1:n.1622C>G
ENST00000698860.1:c.1470C>G	ENSP00000513988.1:p.His490Gln
ENST00000698861.1:c.1458C>G	ENSP00000513989.1:p.His486Gln
ENST00000698862.1:c.*754C>G	ENSP00000513990.1:n.*754C>G
ENST00000698863.1:c.1458C>G	ENSP00000513991.1:p.His486Gln
ENST00000698864.1:n.1673C>G
ENST00000698865.1:c.1479C>G	ENSP00000513992.1:p.His493Gln
ENST00000698866.1:c.*972C>G	ENSP00000513993.1:n.*972C>G
ENST00000698867.1:n.5433C>G
ENST00000698868.1:c.1323C>G	ENSP00000513994.1:p.His441Gln
ENST00000698869.1:c.1311+256C>G	ENSP00000513995.1:n.1311+256C>G
ENST00000698870.1:c.1458C>G	ENSP00000513996.1:p.His486Gln
ENST00000698871.1:n.1981C>G
ENST00000698872.1:c.*247C>G	ENSP00000513997.1:n.*247C>G
ENST00000698873.1:c.*653C>G	ENSP00000513998.1:n.*653C>G
ENST00000698874.1:c.918C>G	ENSP00000513999.1:p.His306Gln
ENST00000698875.1:n.1318C>G
ENST00000698876.1:n.1506C>G
ENST00000698877.1:n.1026C>G
ENST00000698878.1:c.1452C>G	ENSP00000514000.1:p.His484Gln
ENST00000698880.1:c.1326C>G
ENST00000345728.10:c.1458C>G MANE Select	ENSP00000339950.5:p.His486Gln
ENST00000279227.9:c.1470C>G	ENSP00000279227.5:p.His490Gln
ENST00000345728.9:c.1458C>G	ENSP00000339950.5:p.His486Gln
ENST00000541326.5:n.874C>G
ENST00000545896.1:c.146C>G	ENSP00000440209.1:p.Thr49Ser
NM_031471.5:c.1458C>G	NP_113659.3:p.His486Gln
NM_178443.2:c.1470C>G , LRG_180t1:c.1470C>G	NP_848537.1:p.His490Gln
XM_011545294.1:c.1470C>G	XP_011543596.1:p.His490Gln
XM_011545295.1:c.930C>G	XP_011543597.1:p.His310Gln
XM_011545296.1:c.930C>G	XP_011543598.1:p.His310Gln
XM_011545294.3:c.1470C>G	XP_011543596.1:p.His490Gln
XM_011545295.2:c.930C>G	XP_011543597.1:p.His310Gln
XM_017018398.2:c.1458C>G	XP_016873887.1:p.His486Gln
XM_017018399.1:c.918C>G	XP_016873888.1:p.His306Gln
NM_031471.6:c.1458C>G MANE Select	NP_113659.3:p.His486Gln
NM_001382361.1:c.1458C>G	NP_001369290.1:p.His486Gln
NM_001382362.1:c.1470C>G	NP_001369291.1:p.His490Gln
NM_001382363.1:c.918C>G	NP_001369292.1:p.His306Gln
NM_001382364.1:c.930C>G	NP_001369293.1:p.His310Gln
NM_001382448.1:c.1458C>G	NP_001369377.1:p.His486Gln
NM_178443.3:c.1470C>G	NP_848537.1:p.His490Gln