Canonical Allele Identifier: CA381089864

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990606A>T (hg19) ; chr11:g.64223134A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223134A>T , CM000673.2:g.64223134A>T	GRCh38
NC_000011.9:g.63990606A>T , CM000673.1:g.63990606A>T	GRCh37
NC_000011.8:g.63747182A>T	NCBI36
NG_016360.1:g.21455A>T , LRG_180:g.21455A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1769A>T	ENSP00000279227.5:p.Lys590Met
ENST00000540554.2:n.3281A>T
ENST00000541252.2:c.1217A>T	ENSP00000438885.2:p.Lys406Met
ENST00000544997.6:c.1757A>T	ENSP00000445778.2:p.Lys586Met
ENST00000545896.2:c.321A>T	ENSP00000440209.2:p.Gln107His
ENST00000546255.2:n.2061A>T
ENST00000698845.1:c.*952A>T	ENSP00000513981.1:n.*952A>T
ENST00000698846.1:n.2003A>T
ENST00000698847.1:c.*1162A>T	ENSP00000513982.1:n.*1162A>T
ENST00000698850.1:n.3778A>T
ENST00000698852.1:c.1757A>T	ENSP00000513984.1:p.Lys586Met
ENST00000698853.1:c.*986A>T	ENSP00000513985.1:n.*986A>T
ENST00000698854.1:c.*1087A>T	ENSP00000513986.1:n.*1087A>T
ENST00000698855.1:n.3409A>T
ENST00000698856.1:n.3103A>T
ENST00000698859.1:n.2267A>T
ENST00000698860.1:c.1769A>T	ENSP00000513988.1:p.Lys590Met
ENST00000698861.1:c.1757A>T	ENSP00000513989.1:p.Lys586Met
ENST00000698862.1:c.*1053A>T	ENSP00000513990.1:n.*1053A>T
ENST00000698863.1:c.1757A>T	ENSP00000513991.1:p.Lys586Met
ENST00000698864.1:n.2318A>T
ENST00000698865.1:c.1778A>T	ENSP00000513992.1:p.Lys593Met
ENST00000698866.1:c.*1545A>T	ENSP00000513993.1:n.*1545A>T
ENST00000698867.1:n.5732A>T
ENST00000698868.1:c.1622A>T	ENSP00000513994.1:p.Lys541Met
ENST00000698869.1:c.1523A>T	ENSP00000513995.1:p.Lys508Met
ENST00000698870.1:c.1757A>T	ENSP00000513996.1:p.Lys586Met
ENST00000698871.1:n.2280A>T
ENST00000698872.1:c.*546A>T	ENSP00000513997.1:n.*546A>T
ENST00000698873.1:c.*952A>T	ENSP00000513998.1:n.*952A>T
ENST00000698874.1:c.1217A>T	ENSP00000513999.1:p.Lys406Met
ENST00000698875.1:n.1617A>T
ENST00000698876.1:n.1805A>T
ENST00000698877.1:n.1325A>T
ENST00000698878.1:c.1751A>T	ENSP00000514000.1:p.Lys584Met
ENST00000698880.1:c.1625A>T
ENST00000345728.10:c.1757A>T MANE Select	ENSP00000339950.5:p.Lys586Met
ENST00000279227.9:c.1769A>T	ENSP00000279227.5:p.Lys590Met
ENST00000345728.9:c.1757A>T	ENSP00000339950.5:p.Lys586Met
ENST00000545896.1:c.320A>T	ENSP00000440209.1:p.Lys107Met
NM_031471.5:c.1757A>T	NP_113659.3:p.Lys586Met
NM_178443.2:c.1769A>T , LRG_180t1:c.1769A>T	NP_848537.1:p.Lys590Met
XM_011545294.1:c.1769A>T	XP_011543596.1:p.Lys590Met
XM_011545295.1:c.1229A>T	XP_011543597.1:p.Lys410Met
XM_011545296.1:c.1229A>T	XP_011543598.1:p.Lys410Met
XM_011545294.3:c.1769A>T	XP_011543596.1:p.Lys590Met
XM_011545295.2:c.1229A>T	XP_011543597.1:p.Lys410Met
XM_017018398.2:c.1757A>T	XP_016873887.1:p.Lys586Met
XM_017018399.1:c.1217A>T	XP_016873888.1:p.Lys406Met
NM_031471.6:c.1757A>T MANE Select	NP_113659.3:p.Lys586Met
NM_001382361.1:c.1757A>T	NP_001369290.1:p.Lys586Met
NM_001382362.1:c.1769A>T	NP_001369291.1:p.Lys590Met
NM_001382363.1:c.1217A>T	NP_001369292.1:p.Lys406Met
NM_001382364.1:c.1229A>T	NP_001369293.1:p.Lys410Met
NM_001382448.1:c.1757A>T	NP_001369377.1:p.Lys586Met
NM_178443.3:c.1769A>T	NP_848537.1:p.Lys590Met