Canonical Allele Identifier: CA381088499

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63988125A>G (hg19) ; chr11:g.64220653A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220653A>G , CM000673.2:g.64220653A>G	GRCh38
NC_000011.9:g.63988125A>G , CM000673.1:g.63988125A>G	GRCh37
NC_000011.8:g.63744701A>G	NCBI36
NG_016360.1:g.18974A>G , LRG_180:g.18974A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000279227.10:c.1541A>G	ENSP00000279227.5:p.Lys514Arg
ENST00000540554.2:n.2707A>G
ENST00000541252.2:c.989A>G	ENSP00000438885.2:p.Lys330Arg
ENST00000541326.6:n.950A>G
ENST00000544997.6:c.1529A>G	ENSP00000445778.2:p.Lys510Arg
ENST00000545896.2:c.218A>G	ENSP00000440209.2:p.Lys73Arg
ENST00000546255.2:n.1833A>G
ENST00000698845.1:c.*724A>G	ENSP00000513981.1:n.*724A>G
ENST00000698846.1:n.1775A>G
ENST00000698847.1:c.*934A>G	ENSP00000513982.1:n.*934A>G
ENST00000698849.1:n.649A>G
ENST00000698850.1:n.1297A>G
ENST00000698852.1:c.1529A>G	ENSP00000513984.1:p.Lys510Arg
ENST00000698853.1:c.*758A>G	ENSP00000513985.1:n.*758A>G
ENST00000698854.1:c.*859A>G	ENSP00000513986.1:n.*859A>G
ENST00000698855.1:n.3181A>G
ENST00000698856.1:n.2875A>G
ENST00000698859.1:n.1693A>G
ENST00000698860.1:c.1541A>G	ENSP00000513988.1:p.Lys514Arg
ENST00000698861.1:c.1529A>G	ENSP00000513989.1:p.Lys510Arg
ENST00000698862.1:c.*825A>G	ENSP00000513990.1:n.*825A>G
ENST00000698863.1:c.1529A>G	ENSP00000513991.1:p.Lys510Arg
ENST00000698864.1:n.1744A>G
ENST00000698865.1:c.1550A>G	ENSP00000513992.1:p.Lys517Arg
ENST00000698866.1:c.*1043A>G	ENSP00000513993.1:n.*1043A>G
ENST00000698867.1:n.5504A>G
ENST00000698868.1:c.1394A>G	ENSP00000513994.1:p.Lys465Arg
ENST00000698869.1:c.1311+327A>G	ENSP00000513995.1:n.1311+327A>G
ENST00000698870.1:c.1529A>G	ENSP00000513996.1:p.Lys510Arg
ENST00000698871.1:n.2052A>G
ENST00000698872.1:c.*318A>G	ENSP00000513997.1:n.*318A>G
ENST00000698873.1:c.*724A>G	ENSP00000513998.1:n.*724A>G
ENST00000698874.1:c.989A>G	ENSP00000513999.1:p.Lys330Arg
ENST00000698875.1:n.1389A>G
ENST00000698876.1:n.1577A>G
ENST00000698877.1:n.1097A>G
ENST00000698878.1:c.1523A>G	ENSP00000514000.1:p.Lys508Arg
ENST00000698880.1:c.1397A>G
ENST00000345728.10:c.1529A>G MANE Select	ENSP00000339950.5:p.Lys510Arg
ENST00000279227.9:c.1541A>G	ENSP00000279227.5:p.Lys514Arg
ENST00000345728.9:c.1529A>G	ENSP00000339950.5:p.Lys510Arg
ENST00000545896.1:c.217A>G	ENSP00000440209.1:p.Ser73Gly
NM_031471.5:c.1529A>G	NP_113659.3:p.Lys510Arg
NM_178443.2:c.1541A>G , LRG_180t1:c.1541A>G	NP_848537.1:p.Lys514Arg
XM_011545294.1:c.1541A>G	XP_011543596.1:p.Lys514Arg
XM_011545295.1:c.1001A>G	XP_011543597.1:p.Lys334Arg
XM_011545296.1:c.1001A>G	XP_011543598.1:p.Lys334Arg
XM_011545294.3:c.1541A>G	XP_011543596.1:p.Lys514Arg
XM_011545295.2:c.1001A>G	XP_011543597.1:p.Lys334Arg
XM_017018398.2:c.1529A>G	XP_016873887.1:p.Lys510Arg
XM_017018399.1:c.989A>G	XP_016873888.1:p.Lys330Arg
NM_031471.6:c.1529A>G MANE Select	NP_113659.3:p.Lys510Arg
NM_001382361.1:c.1529A>G	NP_001369290.1:p.Lys510Arg
NM_001382362.1:c.1541A>G	NP_001369291.1:p.Lys514Arg
NM_001382363.1:c.989A>G	NP_001369292.1:p.Lys330Arg
NM_001382364.1:c.1001A>G	NP_001369293.1:p.Lys334Arg
NM_001382448.1:c.1529A>G	NP_001369377.1:p.Lys510Arg
NM_178443.3:c.1541A>G	NP_848537.1:p.Lys514Arg